Compounds and methods for regulating bacterial growth and pathogenesis

ABSTRACT

The invention provides autoinducer-2 analogs that regulate the activity of autoinducer-2 and methods of using such analogs for regulating bacterial growth and pathogenesis.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No.60/203,000, filed May 10, 2000 and U.S. Provisional Application No.60/254,398, filed Dec. 7, 2000, both of which are herein incorporated byreference.

STATEMENT OF GOVERNMENT INTEREST

The U.S. Government has certain rights in this invention, which was madein part with funds from the National Science Foundation, Grant No.MCB-9506033.

FIELD OF THE INVENTION

This invention relates to bacterial diseases of humans and othermammals. In particular, the invention provides a novel signaling factorinvolved in regulating bacterial growth and pathogenesis, analogs andderivatives of the signaling factor, and methods for controllingbacterial growth and pathogenesis through use of such analogs andderivatives.

BACKGROUND OF THE INVENTION

Intercellular cooperation confers a considerable advantage onmulticellular organisms that was thought to be unavailable tounicellular organisms such as prokaryotes. Research in the last twentyyears has revealed, however, that prokaryotes can communicate with eachother in a way that modulates gene expression, and thereby can reapbenefits that would otherwise be exclusive to eukaryotes. This abilitywas discovered in luminous marine bacteria such as Vibrio fischeri andVibrio harveyi, which activate the expression of genes involved in lightproduction only when their population density exceeds a critical value.This phenomenon, known as quorum-sensing, is now recognized as a generalmechanism for gene regulation in many Gram-negative bacteria, and itallows them to perform in unison such activities as bioluminescence,swarming, biofilm formation, production of proteolytic enzymes,synthesis of antibiotics, development of genetic competence, plasmidconjugal transfer, and spoliation.

Quorum-sensing bacteria fall into two classes, depending on how manydensity-sensing systems they have. Both classes synthesize, release, andrespond to signaling molecules called autoinducers to control geneexpression as a function of cell density. Bacteria in the larger classuse acyl-homoserine lactone signals in a single density-sensing system,with one gene that encodes an autoinducer synthase, and another thatencodes a transcriptional activator protein that mediates response tothe autoinducer. These genes are homologous to luxI and luxR of V.fischeri, respectively (Bassler and Silverman, in Two component SignalTransduction, Hoch et al., eds, Am. Soc. Microbiol. Washington D.C., pp431-435, 1995).

Many bacteria that use the autoinducer-1 signaling factor associate withhigher organisms, i.e., plants and animals, at some point during theirlifecycles. For example, Pseudomonas aeruginosa, an opportunisticpathogen in humans with cystic fibrosis, regulates various virulencedeterminants with autoinducer-1. Other examples ofautoinducer-1-producing bacteria include Erwinia carotovora, Pseudomonasaureofaciens, Yersinia enterocolitica, Vibrio harveyi, and Agrobacteriumtumefaciens. E. carotovora infects certain plants and creates enzymesthat degrade the plant's cell walls, resulting in what is called “softrot disease.” Yersinia enterocolitica causes gastrointestinal disease inhumans and reportedly produces an autoinducer. P. aureofacienssynthesizes antibiotics under autoinducer control that block fungusgrowth in the roots.

Bacteria of the other class, exemplified by V. harveyi, have not one buttwo independent density-sensing systems. V. harveyi apparently uses themore species-specific Signaling System 1 for intra-speciescommunication, and the less species-selective Signaling System 2 forinter-species communication (Bassler et al., J. Bacteriol. 179:4043-4045, 1997). Each system comprises a sensor-autoinducer pair;Signaling System 1 uses Sensor 1 and autoinducer-1 (AI-1), whileSignaling System 2 uses Sensor 2 and autoinducer-2 (AI-2) (Bassler etal., Mol. Microbiol. 13: 273-286, 1994). While autoinducer-1 isN-(3-hydroxy butanoyl)-L-homoserine lactone (HSL) (see Bassler et al.,Mol. Microbiol. 9: 773-786, 1993), the structure of autoinducer-2 hasnot been established, nor have the gene(s) involved in its biosynthesisbeen identified.

Recent research indicates that quorum-sensing takes place not only amongluminous marine bacteria, but also among pathogenic bacteria, where itregulates the production of virulence factors that are critical factorsin bacterial pathogenesis. Thus, it would be an advance in the art toidentify and characterize compounds with autoinducer-2 activity and thegenes encoding the proteins required for production of thenaturally-occurring autoinducer-2. Such an advance would provide a wayto identify compounds useful for controlling pathogenic bacteria, a wayto augment traditional antibiotic treatments, and a new target for thedevelopment of new antimicrobial agents.

SUMMARY OF THE INVENTION

The applicants have now discovered that many bacteria, including somenon-luminous pathogens, secrete a signaling molecule that mimics V.harveyi autoinducer-2 in its function and physical properties. Bacteriathat produce the AI-2 signaling factor of the invention include Vibrioharveyi, Vibrio cholerae, Vibrio parahaemolyticus, Vibrio alginolyticus,Pseudomonas phosphoreum, Yersinia enterocolitica, Escherichia coli,Salmonella typhimurium, Haemophilus influenzae, Helicobacter pylori,Bacillus subtilis, Borrelia burgfdorferi, Neisseria meningitidis,Neisseria gonorrhoeae, Yersinia pestis, Campylobacter jejuni,Deinococcus radiodurans, Mycobacterium tuberculosis, Enterococcusfaecalis, Streptococcus pneumoniae, Streptococcus pyogenes andStaphylococcus aureus.

Free-living bacteria produce this novel signaling molecule only uponshifting to a colonizing, and therefore potentially pathogenic,existence in a host organism. Thus, in addition to stimulatingluminescence genes in V. harveyi, the signaling molecule is expected tostimulate genes related to pathogenesis in bacteria that produce it. Inaddition to a purified molecule with autoinducer-2 signaling activity,the invention provides a synthetic form of the molecule and derivativesof it that regulate bacterial growth and pathogenesis.

In another aspect, there is provided a method for regulating theactivity of an autoinducer-2 receptor comprising contacting anautoinducer-2 receptor with an AI-2 agonist or antagonist compound.

In another aspect, the invention provides a method of regulatingautoinducer-2 activity by contacting a bacterial cell comprisingautoinducer-2, or extract thereof, with a compound of structure I, II,III or IV.

In yet another aspect, the invention provides a method for regulatingautoinducer-2 receptor activity by contacting an autoinducer-2 receptorwith a compound of structure I, II, III or IV.

In another aspect, the invention provides a method for controllingbacterial growth or virulence by identifying a subject infected with anautoinducer-2-producing bacterium and administering to the subject acompound of structure I, II, III or IV.

In yet another aspect, the invention provides a method for inhibitingbacterial growth or virulence in a subject, by identifying a subject inwhich bacteria are producing autoinducer-2 and administering to thesubject an inhibitor of an autoinducer-2 of the present invention.

In another aspect, the invention provides a method for identifying acompound that regulates the activity of autoinducer-2 by comparing theactivity of autoinducer-2 obtained in the presence of the compound tothat obtained in its absence.

In another aspect, the invention provides a method for identifying anautoinducer analog by contacting a cell, or cell extract, that producesa detectable amount of light in response to an autoinducer with theautoinducer analog and comparing the amount of light produced in thepresence and the absence of the autoinducer analog.

In another aspect, the invention provides a method for identifying acompound that regulates the production or activity of autoinducer-2 bycontacting with the compound a cell that produces autoinducer-2, anddetermining whether autoinducer-2 activity is present in the cell.

In another aspect, the invention provides a method for identifying acompound that affects binding of autoinducer-2 to an autoinducer-2receptor by: (a) contacting autoinducer-2 and the autoinducer-2 receptorwith the compound; (b) contacting (a) with a cell, or cell extract, thatproduces light in response to autoinducer-2 binding to the autoinducer-2receptor; and (c) measuring the effect of the compound on lightproduction.

In yet another aspect, the invention provides a method for identifying acompound that affects autoinducer-2 binding to an autoinducer-2 receptorby: (a) contacting with the compound a complex formed betweenautoinducer-2 and the autoinducer-2 receptor to allow dissociation ofthe complex; (b) contacting (a) with a cell, or cell extract thereof,that produces light in response to binding of autoinducer-2 to theautoinducer-2 receptor; and (c) measuring the effect of the compound onlight production.

In yet another aspect, the invention provides a method for regulatingexpression of a siderophore in a bacterial cell by contacting a cellcapable of producing the siderophore with a compound of structure I, II,III or IV.

In another aspect, the invention provides a method for regulatingexopolysaccharide production in a cell by contacting a cell capable ofproducing an exopolysaccharide with a compound of structure I, II, IIIor IV.

In another aspect, the invention provides a method for regulatingbacterial colony morphology by contacting a bacterial colony with acompound of structure I, II, III or IV.

In another aspect, the invention provides a method for regulatingbacterial biofilm formation by contacting a bacterium capable of biofilmformation with any combination of compounds set forth in structuresI-IV.

In another aspect, the invention provides a method for producingautoinducer-2 by contacting S-adenosylhomocysteine (SAH) with a LuxSprotein.

In another aspect, the invention further provides a method for producingautoinducer-2 by; a) contacting S-adenosylhomocysteine (SAH) with a5′-methylthioadenosine/S-adenosylhomocysteine nucleosidase (pfs) proteinto form S-ribosylhomocysteine; b) contacting the S-ribosylhomocysteinefrom a) with a LuxS protein to promote the conversion ofS-ribosylhomocysteine to autoinducer-2.

In yet another aspect, the invention further provides a method fordetecting an autoinducer-associated biomarker by: (a) contacting atleast one cell with an autoinducer to promote induction of a biomarker;and (b) detecting the biomarker.

In another aspect, the invention provides a method for regulatingbacterial cell growth or expression of a virulence factor comprisingcontacting a bacterial cell with an isolated autoinducer-2 analogcomprising the structure:

The invention further provides a synergistic antibiotic compositioncomprising an antibiotic and an inhibitor of the quorum-sensing pathwayof a microorganism.

The invention further provides a medical device comprising a synergisticantibiotic composition comprising an antibiotic and an inhibitor of thequorum-sensing pathway of a microorganism, as well as a method oftreating infections in a warm-blooded animal caused by microorganismspossessing a quorum-sensing mechanism, comprising administering to theanimal a therapeutically effective amount of the synergistic antibioticcomposition.

The invention further provides a pharmaceutical composition comprising asynergistic antibiotic composition comprising an antibiotic and aninhibitor of a quorum-sensing pathway of a microorganism or apharmaceutically acceptable salt thereof and one or morepharmaceutically acceptable carriers, adjuvants or vehicles.

The invention also provides a method of treating infections in awarm-blooded animal caused by microorganisms possessing a quorum-sensingmechanism that comprises administering to the animal a therapeuticallyeffective amount of the synergistic antibiotic composition comprising anantibiotic and an inhibitor of the quorum-sensing pathway of amicroorganism.

The invention further provides a method for inhibiting biofilm formationby contacting a bacterium capable of biofilm formation with a compoundhaving the structure set forth in structure III or structure IV.

The invention further provides a medical device comprising at least oneantimicrobial compound having the structure set forth in structure IIIor structure IV, where the device is supplemented with the compound andthe compound is present in a concentration sufficient to provide alocalized antimicrobial effect.

The invention further provides a medical device comprising at least onesynergistic antibiotic composition of an antibiotic and an inhibitor ofthe quorum-sensing pathway of a microorganism, where the composition ispresent in a concentration sufficient to provide a localizedantimicrobial effect.

The invention further provides a medical device comprising at least onepharmaceutical composition comprising a synergistic antibioticcomposition comprising an antibiotic and an inhibitor of aquorum-sensing pathway of a microorganism or apharmaceutically-acceptable salt thereof and one or morepharmaceutically acceptable carriers, adjuvants or vehicles, wherein thecomposition is present in a concentration sufficient to provide alocalized anti-microbial effect.

Additional features and advantages of the present invention will bebetter understood by reference to the drawings, detailed description andexamples that follow.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Signaling substance from E. coli AB1157 and S. typhimurium LT2cell-free culture fluids that induces luminescence in V. harveyi. Theresponses of V. harveyi reporter strains BB170 (Sensor 1⁻, Sensor 2⁺)(FIG. 1A), and BB886 (Sensor 1⁺, Sensor 2⁻) (FIG. 1B) to signalingsubstances present in cell-free culture fluids from E. coli, S.typhimurium and V. harveyi strains are shown. A bright culture of eachreporter strain was diluted 1:5000 into fresh medium, and the lightproduction per cell was then measured during the growth of the dilutedculture. Cell-free culture fluids or sterile growth medium were added ata final concentration of 10% (v/v) at the start of the experiment. Thedata for the 5-hour time point are shown and are presented as thepercent of the activity obtained when V. harveyi cell-free spent culturefluids are added. Abbreviations used for the different strains are: V.h;Vibrio harveyi, S.t; Salmonella typhimurium, and E.c; Escherichia coli.

FIG. 2. Secretion of the autoinducer-2 signaling molecule by viable E.coli and S. typhimurium. The response of the V. harveyi reporter strainBB170 (Sensor 1⁻, Sensor 2⁺) to a signaling substance produced andsecreted by E. coli AB1157. and S. typhimurium LT2 but not E. coli DH5αis shown. V. harveyi reporter strain BB170 was diluted 1:5000 in ABmedium and light output per cell was monitored during growth. At thestart of the experiment, either 1×10⁶ E. coli AB1157, S. typhimurium LT2or E. coli DH5α washed and resuspended viable cells (left-hand, whitebars) or UV-killed cells (right-hand, black bars) was added. The dataare presented as the fold-activation above the endogenous level ofluminescence expressed by V. harveyi BB170 at the 5-hour time point.Abbreviations used for the different strains are: S.t; Salmonellatyphimurium, and E.c; Escherichia coli.

FIG. 3. Effect of glucose depletion on the production and degradation ofthe autoinducer-2 signaling activity by S. typhimurium LT2. S.typhimurium LT2 was grown in LB medium containing either 0.1% glucose(FIG. 3A) or 0.5% glucose (FIG. 3B). At the specified times cell-freeculture fluids were prepared and assayed for signaling activity in theluminescence stimulation assay (Bars), and the concentration of glucoseremaining (circles). The cell number was determined at each time bydiluting and plating the S. typhimurium LT2 on LB medium and countingcolonies the next day (squares). The signaling activity is presented asthe percent of the activity obtained when V. harveyi cell-free spentculture fluids are added. These data correspond to the 5 h time point inthe luminescence stimulation assay. The glucose concentration is shownas % glucose remaining. Cell number is cells/ml×10⁻⁹. The symbol \\indicates that the time axis is not drawn to scale after 8 h.

FIG. 4. Response curve of V. harveyi to AI-2 produced by V. harveyi andS. typhimurium. The V. harveyi reporter strain BB170 (Sensor 1⁻, Sensor2⁺) was tested for its response to the addition of exogenous AI-2 madeby V. harveyi strain BB152 (AI-1⁻, AI-2⁺) and to that made by S.typhimurium LT2. A bright culture of the reporter strain was diluted1:5000 and either 10% (v/v) growth medium (closed circles), cell-freeculture fluid from V. harveyi BB152 grown overnight in AB (opencircles), or cell-free culture fluid from S. typhimurium LT2 grown for 6h on LB+0.5% glucose (closed squares) was added at the start of theexperiment. RLU denotes relative light units and is defined as (countsmin⁻¹×10⁻³)/(colony-forming units ml¹).

FIG. 5. Conditions affecting autoinducer production in S. typhimurium.S. typhimurium LT2 was subjected to a variety of treatments after whichcell-free culture fluids or osmotic shock fluids were prepared. Thesepreparations were added to a diluted culture of the V. harveyi AI-2reporter strain BB170 at 10% (v/v) and light output was measuredthereafter. Fold activation is the level of light produced by thereporter following addition of the specified S. typhimurium preparationdivided by the light output of the reporter when growth medium alone wasadded. The bars in FIG. 5A represent cell-free fluids prepared from S.typhimurium after the following treatments: LB 6 h; 6 h growth in LB at30° C., LB+Glc 6 h; 6 h growth in LB+0.5% glucose at 30° C., LB+Glc 24h; 24 h growth in LB+0.5% glucose at 30° C. In all the experimentspresented in FIG. 5B, the S. typhimurium were pre-grown at 30° C. for 6h in LB containing 0.5% glucose, then pelleted and resuspended for 2 hunder the following conditions: LB; in LB at 30° C., LB+Glc; in LB+0.5%glucose at 30° C., LB pH 5; in LB at pH 5.0 at 30° C., 0.4 M NaCl; in0.4 M NaCl at 30° C., 0.1M NaCl; in 0.1M NaCl at 30° C., and Heat Shock43°; in LB+0.5% glucose at 43° C. After these two-hour treatments,cell-free fluids were prepared from each sample and assayed.

FIG. 6. S. typhimurium signaling activity in limiting and non-limitingconcentrations of glucose. S. typhimurium LT2 was grown in LB in thepresence of limiting (0.1%) and non-limiting (1.0%) concentrations ofglucose. The activity present in the cell-free culture fluids (blackbars) was assayed at the times indicated and normalized to that producedby 1×10⁹ cells. The increase in signaling activity measured in the 0.4 MNaCl osmotic shock fluids prepared from the same cells is shown as thewhite bars on top of the black bars. These data are also normalized for1×10⁹ cells. The signaling activity for limiting glucose is shown inFIGS. 6A, 6C, and 6E, and that for non-limiting glucose is shown inFIGS. 6B, 6D, and 6F. FIGS. 6A and 6B also show the percent glucoseremaining (triangles), FIGS. 6C and 6D show the cell number (squares),and Panels E and F show the pH (circles) at each time point.

FIG. 7. Effects of glucose and pH on signal production by S.typhimurium. The quorum-sensing signal released by S. typhimurium LT2was measured when the cells were grown in LB medium containing 0.5%glucose at pH 7.2 (FIG. 7A, bars), and when the cells were grown in LBat pH 5.0 without an added carbon source (FIG. 7B, bars). The level ofsignal present in cell free culture fluids (black bars) and in 0.4 MNaCl osmotic shock fluids was measured (white bars on top of black bars)at the time points indicated. In each panel, the circles represent thepH of the medium, and the squares show the cell number at the differenttime points.

FIG. 8. High osmolarity induces signal release and low osmolarityinduces signal degradation in S. typhimurium LT2. The quorum-sensingsignal released by S. typhimurium LT2 resuspended in 0.4 M NaCl and in0.1M NaCl was measured in the presence and absence of protein synthesis.S. typhimurium LT2 was pre-grown in LB containing 0.5% glucose for 6 h.The cells were harvested and resuspended in 0.4 M NaCl (FIG. 8A) or 0.1M NaCl (FIG. 8B) in the presence or absence of 30 g/ml Cm for the timeperiods indicated. In each panel, the open symbols represent theactivity measured in the absence of Cm and the closed symbols representthe activity measured in the presence of Cm.

FIG. 9. The luxS and ygaG genes from V. harveyi and E. coli MG1655. FIG.9A shows a restriction map of the V. harveyi luxS_(V.h.) chromosomalregion which was defined by Tn5 insertion. The sites of Tn5 insertionsthat disrupted the AI-2 production function and one control Tn5insertion outside of the luxS_(V.h.) locus are shown (triangles). FIG.9B depicts the ygaG region in the E. coli MG1655 chromosome. This ORF isflanked by the emrB and gshA genes. The direction of transcription ofeach gene is indicated by the horizontal arrows. The correspondingposition of the MudJ insertion that eliminated AI-2 production in S.typhimurium LT2 is shown by a vertical arrow. H, R, P, and B denoteHindIII, EcoRI, PstI and BamHI restriction sites, respectively.

FIG. 10 shows autoinducer production phenotypes of V. harveyi and S.typhimurium strains. Cell-free culture fluids from V. harveyi and S.typhimurium strains were prepared and tested for AI-2 activity in the V.harveyi BB170 bioassay. FIG. 10A: AI-2 production phenotypes of the wildtype V. harveyi strain MM28 which contains a Tn5 insertion outside ofluxS_(V.h.) (denoted WT) and the luxS_(V.h.)::Tn5 mutant strain MM30(denoted luxS⁻). FIG. 10B: AI-2 production phenotypes of wild type S.typhimurium LT2 (denoted WT) and the ygaG::MudJ insertion mutant strainCS132 (denoted ygaG⁻). Activity is reported as fold-induction ofluminescence expression of the V. harveyi BB170 reporter strain overthat when sterile medium was added.

FIG. 11 is a graph showing complementation of AI-2 production in S.typhimurium CS132 and E. coli DH5α. Cell-free culture fluids from E.coli and S. typhimurium strains were tested for AI-2 activity in thebioassay. The activity present in these fluids was compared to thatproduced by wild type V. harveyi BB120. In the figure, the level ofBB120 activity was normalized to 100%. FIG. 11A: AI-2 activity incell-free fluids from wild type V. harveyi BB120, E. coli O157:H7, andS. typhimurium LT2. FIG. 11B: Complementation of S. typhimurium CS132(ygaG::MudJ) and FIG. 11C: Complementation of E. coli DH5α. In Panel Band C, the in trans AI-2 production genes are the following: vectorcontrol (denoted: none), E. coli O157:H7 ygaG; and V. harveyi BB120luxS_(V.h.) E. coli and V. harveyi are abbreviated _(E.c.) and _(V.h.),respectively.

FIG. 12 shows the alignment of LuxS and YgaG protein sequences. Thetranslated protein sequences for the AI-2 production family of proteinsare shown. We determined the sequences for the luxS_(V.h.) gene from V.harveyi BB120 (SEQ ID NO: 10), and the ygaG genes (re-named herein asluxS_(E.c.) from E. coli MG1655 (SEQ ID NO: 25), E. coli O157:H7 (SEQ IDNO: 11), and E. coli DH5α (SEQ ID NO: 26). The S. typhimurium LT2 ygaG(re-named herein luxS_(S.t.) partial sequence came from the S.typhimurium database. Amino acid residues that are not identical to theLuxS_(V.h.) protein are underlined and not in bold font. The site of theframe shift mutation in the E. coli DH5α DNA sequence is denoted by an“*.” The 20 altered amino acid residues that are translated followingthe frame shift are enclosed by the box.

FIG. 13 provides a diagram of.the hybrid quorum-sensing circuit ofVibrio harveyi. The AI-1 and AI-2 circuits are independently stimulatedbut integrate their signals for light expression. Each pathway, however,is also independently competent to generate light. This allows forreciprocal mutations in the LuxN or LuxQ sensors to be used to constructa reporter specific for AI-2 or AI-1, respectively.

FIG. 14 is a graph representing response phenotypes of V. harveyi wildtype and lux regulatory mutants. At the first time point, cell-freeculture fluids (10%), or nothing (N.A.) was added. Wild type, cell-freeculture fluid (AI-1+AI2); LuxS⁻ cell-free culture fluid (AI-1); LuxM⁻cell-free culture fluid (AI-2). Relative light units are defined ascpm×10³/CFU/ml.

FIG. 15 shows a diagram of the biosynthetic pathway of autoinducer-2(AI-2).

FIG. 16 shows bar graphs indicating the result of luminescence screeningassays of AI-2 analogs. FIG. 16 panels A and B show the results of a 6hour assay using compounds 6, 9, 15 and 18 (panel A) and compounds 3, 4,7 and 13 (panel B) on test strain BB170. FIG. 16 panels C and D show theeffect of the same compounds on control strain JAF78.

FIG. 17 shows examples of structures of analog compounds that inhibitthe activity of AI-2 in the V. harveyi luminescence assay. Thestructures of these compounds indicate that the C2 and C3 positions areimportant to the inhibitory activity of the compounds.

FIG. 18 is a bar graph showing the effect of compounds QXP009, QXP010,QXP015 and QXP018 on AI-2 activity in the V. harveyi luminescence assay.

FIGS. 19A, 19B and 19C show a list of compounds and their effect on AI-2activity in the V. harveyi luminescence assay.

FIG. 20 is a photograph showing σ⁵⁴ and LuxO regulation of colonymorphology in V. harveyi. The smooth and rugose colony morphologies ofdifferent V. harveyi strains are shown in the photographs. Each V.harveyi strain was grown in LM broth overnight at 30° C. The strainswere streaked onto LM plates, grown for 24 hr at 30° C. andphotographed. The strain denotations are the following: wt, BB120; luxOD47E, JAF548; rpoN::Cmr, BNL240; and luxO D47E, rpoN::Cmr, BNL244. BothBNL240 and BNL244 were supplemented with 1 mM L-glutamine in broth andon plates.

FIG. 21 shows the effect of compound QXP031 on bioluminescence intensityin V. harveyi tester strain. The results are normalized to cell countand control strain. Results demonstrate up to 15000 fold specificdecrease in bioluminescence as a result of AI-2 inhibition at variouscompound QXP031 concentrations.

FIG. 22 shows a CAMP assay indicating inhibition of CAMP expression bycompound QXP031. The horizontal streak is S. aureus 25923 and thevertical streaks are S. pyogenes 19615. Filter disks containing eitherDMSO no drug control or compound QXP031 were applied to plates andincubated anaerobically overnight at 37° C. No compound control resultsin a positive CAMP score as indicated by the arrow shaped region ofcomplete beta-hemolysis. Application of QXP031 results in a completeinhibition of hemolysis.

FIG. 23 shows inhibition proteolysis of milk protein by compound QXP031((R)-4-acetoxy-cyclopent-2-eneone). Skim milk containing plates wereoverlaid with top agar containing S. pyogenes 19615. Filter diskscontaining either DMSO no compound control or compound QXP031 wereapplied to plates and incubated anaerobically overnight at 37° C. Asshown in FIG. 23, the entire plate clears due to S. pyogenes proteolyticactivity except for the zone surrounding the QXP031 containing discwhere proteolysis was inhibited.

FIG. 24 shows induction of bioluminescence by synthetic4-hydroxy-5-methyl-2h-furan-3-one. The MM32 indicator strain (LuxS−,LuxN−) of V. harveyi was incubated with various doses of AI-2 and thebioluminescence signal measured at various time points during a 6-hourincubation.

FIG. 25 shows biofilm formation for wild-type V. harveyi (strain BB120),strain MM32 (LuxN−, LuxS−) and V. harveyi indicator strain BB170(LuxN−). The strains were tested for biofilm formation using either ABmedia with supplemented with glucose (ABG; Panel A) or LB mediasupplemented with glucose (LBG; Panel B). Absorbance reading at 600 nm(A600) were used to measure the amounts of crystal violet adhered to thebiofilm.

FIG. 26 shows V. harveyi biofilm formation in response to increasingamounts of 4-hydroxy-5-methyl-2h-furan-3-one. The final concentration ofAI-2 in each assay is indicated.

FIG. 27 shows Pseudomonas aeruginosa biofilm formation in response toAI-2. Pseudomonas aeruginosa (ATCC 27853) were tested for biofilmformation using AB media supplemented with glucose (LBG). Absorbancereading at 600 nm (A600) were used to measure the amounts of crystalviolet adhered to the biofilm. Doses in the legend refer to the finalconcentration of AI-2 in the assay.

FIG. 28 shows a BB170 assay measuring the effect of QXP-048(2-methoxy-2,4-diphenyl-3(2H)furanone) on the bioluminescence signalemanating from endogenously produced autoinducer-2. QXP-048 was added atthe outset of the assay at a final concentration of 25 μg/ml.

FIG. 29 shows a BB170 Assay measuring the effect of QXP-048 on signalfrom an exogenous autoinducer-2 signal. Exogenous syntheticautoinducer-2 was added at the outset of the assay at a finalconcentration of 25 μg/ml. QXP-048 was added at the outset of the assayat a final concentration of 25 μg/ml.

FIG. 30 shows an MM32 assay further identifying the inhibitorycapability of compound QXP-048. Exogeneous synthetic autoinducer-2 wasadded at the outset of the assay to a final concentration of 25 μg/ml.QXP-048 was added at the outset of the assay at a final concentration of25 μg/ml.

FIG. 31 shows inhibition of bioluminescence by compound QXP-035. Variousamounts of QXP-035 were used in BB170-based AI-2-dependentbioluminescence assay (indicated in micrograms/milliliter in the figurelegend) and the effects on bioluminescence monitored over time.

FIG. 32 shows the effect of compound QXP-035(2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone) on cell growth.Streptococcus pyogenes ATCC 19615 was grown in the presence of either2.4 μg/ml or 2.5 mg/ml of compound QXP-035. Cell growth was monitored bytaking periodic measurements of absorbance at 600 nm.

FIG. 33 are examples of inhibitory (Column A) and stimulatory (Columns Band C) compounds for the AI-2 receptor.

FIG. 34 are examples of stimulatory compounds for the AI-2 receptor.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

“Lower alkyl” refers to alkyl groups have from one to about ten carbonatoms.

“Isomer” means stereoisomers, and includes enantiomers anddiastereomers.

“Purified from a native source” includes autoinducer-2 analogs that havebeen manufactured by an organism, and includes isolating anautoinducer-2 analog from the culture medium or cytoplasm of bacteriasuch as S. typhimurium through use of conventional purificationtechniques.

“Inhibiting infectivity” includes methods of affecting the ability of apathogenic organism to initially infect or further infect a subject thatwould benefit from such treatment.

“Biomarker” refers to any bacterial cell component that is identifiableby known microscopic, histological, or molecular biological techniques.Such a biomarker can be, for example, a molecule present on a cellsurface, a protein, a nucleic acid, a phosphorylation event, or anymolecular or morphological characteristic of a bacterial cell thatchanges when the bacterium is in the presence of an autoinducer.

A “probe” can be a nucleic acid, protein, small molecule, or antibodyuseful for detecting a bacterial biomarker present in a sample.

As used herein, the term “medical device” means a device having surfacesthat contact tissue, blood, or other bodily fluids in the course oftheir operation. This definition includes within its scope, for example,surgical implants, surgical sutures, wound dressings, extracorporealdevices for use in surgery such as blood oxygenators, blood pumps, bloodsensors, tubing used to carry blood and the like which contact bloodwhich is then returned to the subject. The definition includes withinits scope endoprostheses implanted in blood contact in a human or animalbody such as vascular grafts, stents, pacemaker leads, heart valves, andthe like that are implanted in blood vessels or in the heart. Thedefinition also includes within its scope devices for temporaryintravascular use such as catheters, guide wires, and the like which areplaced into the blood vessels or the heart for purposes of monitoring orrepair.

A “compound” can be any agent, composition, or molecule that affects theactivity of AI-2 or affects the activity of a protein that binds withAI-2. For example, a compound of the invention can be a nucleic acid, aprotein, an analog of AI-2 or small molecule. A “compound” includesmolecules that regulate the autoinducer-2 receptors, such as LuxP orLuxQ. For example, a compound of Structure I, II, III or IV can regulatethe activity of a LuxP protein, a LuxQ protein, a LuxP-LuxQ complex, aLuxP-AI-2 complex, or a LuxP-LuxQ-AI-2 complex, such that bacterialgrowth or the expression of an extracellular virulence factor isregulated. Such compounds include inhibitors that interact directly withAI-2 such that AI-2 is prevented from acting as a sensor forquorum-sensing Signaling System-2. For example, a compound of theinvention could interact directly with 4,5-dihydroxy-2-cyclopenten-1-oneor 4-hydroxy-5-methyl-2h-furan-3-one.

AI-2 “inhibitor” refers to molecules that interfere with the ability ofthe autoinducer to act as a signal for luminescence, bacterial growth orpathogenesis, and includes molecules that degrade or bind to AI-2.Inhibitors also include those compounds that regulate AI-2 activity byinteracting with those proteins normally associated with bacterialgrowth.

The “activity” of AI-2 encompasses any aspect of AI-2's ability to actas a signaling factor in bacterial quorum sensing, growth regulation,and pathogenesis.

“Autoinducer-2 analog” means any compound with at least 10% of theautoinducer-2 activity of any stereoisomer of4-hydroxy-5-methyl-2H-furan-3-one, and includes the naturally-occurringautoinducer-2.

“Signaling factor,” “signaling molecule,” “autoinducer,” and morespecifically, “autoinducer-2,” or “AI-2” all refer to the novelsignaling factor of the present invention. The terms “autoinducer-2” and“AI-2” refer specifically to the signaling factor involved in quorumsensing system 2. The terms “signaling factor” or “signaling molecule,”“autoinducer” or “AI-2-like molecule” refer generally to the signalingfactors of the present invention, of which AI-2 is an example.

“Isolated nucleic acid”, when applied to DNA, refers to a DNA moleculethat is separated from sequences with which it is immediately contiguous(in the 5′ and 3′ directions) in the naturally occurring genome of theorganism from which it was derived. For example, the “isolated nucleicacid” may comprise a DNA molecule inserted into a vector, such as aplasmid or virus vector, or integrated into the genomic DNA of aprocaryote or eucaryote. An “isolated nucleic acid molecule” may alsocomprise a cDNA molecule.

“Isolated nucleic acid” primarily refers to an RNA molecule encoded byan isolated DNA molecule as defined above. Alternatively, the term mayrefer to an RNA molecule that has been sufficiently separated from RNAmolecules with which it would be associated in its natural state (i.e.,in cells or tissues), such that it exists in a “substantially pure” form(the term “substantially pure” is defined below).

“Isolated protein” or “isolated and purified protein” refers primarilyto a protein produced by expression of an isolated nucleic acid moleculeof the invention. Alternatively, this term may refer to a protein thathas been sufficiently separated from other proteins with which it wouldnaturally be associated, to exist in “substantially pure” form.

“Substantially pure” refers to a preparation comprising at least 50-60%by weight the factor of interest (e.g., pathogenesis signaling factor,nucleic acid, oligonucleotide, or protein). More preferably, thepreparation comprises at least 75% by weight, and most preferably 90-99%by weight, the factor of interest. Purity is measured by methodsappropriate for the factor of interest (e.g., chromatographic methods,agarose or polyacrylamide gel electrophoresis, HPLC analysis, and thelike).

“Immunologically specific” refers to antibodies that bind to one or moreepitopes of a protein of interest, but that do not substantiallyrecognize and bind other molecules in a sample containing a mixedpopulation of antigenic biological molecules.

“Specifically hybridizing” refers to the association between twosingle-stranded nucleotide molecules of sufficiently complementarysequence to permit such hybridization under pre-determined conditionsgenerally used in the art (sometimes termed “substantiallycomplementary”). In particular, the term refers to hybridization of anoligonucleotide with a substantially complementary sequence containedwithin a single-stranded DNA or RNA molecule of the invention, to thesubstantial exclusion of hybridization of the oligonucleotide withsingle-stranded nucleic acids of non-complementary sequence.

“Promoter region” refers to the transcriptional regulatory regions of agene, which may be found at the 5′ or 3′ side of the coding region, orwithin the coding region, or within introns.

“Selectable marker gene” refers to a gene encoding a product that, whenexpressed, confers a selectable phenotype such as antibiotic resistanceon a transformed cell.

“Reporter gene” refers to a gene that encodes a product that is easilydetectable by standard methods, either directly or indirectly.

“Operably linked” means that the regulatory sequences necessary forexpression of the coding sequence are placed in the DNA molecule in theappropriate positions relative to the coding sequence to enableexpression of the coding sequence. This same definition is sometimesapplied to the arrangement of transcription units and other regulatoryelements (e.g., enhancers or translation regulatory sequences) in anexpression vector.

“Autoinducer-associated bacterial biomarker” refers to any bacterialcell component that an autoinducer regulates, modifies, enhances,inhibits, or induces.

The term “regulate” has its usual meaning, but also encompasses themeanings of the words enhance, inhibit, and mimic. In addition, as usedherein, the term “expression” when used in connection with a gene suchas LuxP, LuxQ or a gene encoding a virulence factor, has its usualmeaning, but also encompasses the transcription of the gene, thelongevity of functional mRNA transcribed from the gene, the translationof that mRNA, and the activity of the gene product. “Regulating”encompasses inhibition or activation of the autoinducer-2 signalingpathway.

“Antibody” includes intact molecules of polyclonal or monoclonalantibodies, as well as fragments thereof, such as Fab and F(ab′)2,. Forexample, monoclonal antibodies are made from antigen containingfragments of a protein by methods well known to those skilled in the art(Kohler et al., Nature, 256:495, 1975).

“Substantially the same” refers to nucleic acid or amino acid sequenceshaving sequence variation that do not materially affect the nature ofthe protein (i.e., the structural characteristics and/or biologicalactivity of the protein). With particular reference to nucleic acidsequences, the term “substantially the same” refers to the coding regionand-to conserved sequences governing expression, and refers primarily todegenerate codons encoding the same amino acid, or alternate codonsencoding conservative substitute amino acids in the encoded polypeptide.With reference to amino acid sequences, the term “substantially thesame” refers generally to conservative substitutions and/or variationsin regions of the polypeptide not involved in determination of structureor function. The terms “percent identity” and “percent similarity” arealso used herein in comparisons among amino acid sequences. These termsare defined as in the UWGCG sequence analysis program (Devereaux et al.,Nucl. Acids Res. 12: 387-397, 1984), available from the University ofWisconsin, and the parameters used by that program are the parameters tobe used herein to compare sequence identity and similarity.

“Antibiotic” includes bactericidal, as well as bacteristatic agents, andincludes sulfonamides, anti-urinary tract agents, β-lactam antibiotics,cephalosporins, clavulanic acid derivatives, aminoglycosides,tetracylines and related antibacterial agents, macrolides,anti-tuberculosis drugs, anti-Mycobacterium avium agents, anti-leprosyagents, antifungal agents and antiviral agents.

“Sulfonamides” includes sulfanilamide, sulfamethoxazole, sulfacetamide,sulfadiazine, sulfisoxazole, para-aminobenzoic acid and the like, aswell as trimethoprim-sulfamethoxazole.

“Quinolones” means nalidixic acid, cinoxacin, norfloxacin,ciprofloxacin, ofloxacin, sparfloxacin, lomefloxacin, fleroxacin,pefloxacin, amifloxacin and the like.

“Anti-urinary tract infectives” means methenamine, nitrofurantoin andthe like.

By “β-lactam antibiotics” we mean penicillins, cephalosporins and thelike. By penicillins, examples are penicillin G, penicillin V,methicillin, oxacillin, cloxacillin, dicloxacillin, nafcillin,ampicillin, amoxicillin, carbenicillin, carbenicillin indanyl,ticarcillin, mezlocillin, piperacillin, bacampicillin and the like.

“Cephalosporins” means compounds such as cephalothin, cefazolin,cephalexin, cefadroxil, cefamandole, cefoxitin, cefaclor, cefuroxime,cefuroxime axetil, loracarbef, cefonicid, cefotetan, ceforanide,cefotaxime, cefpodoxime proxetil, ceftizoxime, ceftriaxone,cefoperazone, ceftazidime, cefepime, moxalactam and the like. Bycarbapenems we mean beta-lactam antibiotics such as imipenem, meropenem,aztreonam (imipenem-cilastatin).

“Clavulanic acid derivatives” means combinations of amoxicillin andclavulanic acid and ticarcillin and clavulanic acid.

“Aminoglycosides” means streptomycin, gentamicin, tobramycin, amikacin,netilmicin, kanamycin, neomycin and the like.

“Tetracylines” means chlortetracycline, oxytetracycline, demeclocycline,methacycline, doxycycline, minocycline and the like.

“Related antibacterial agents” means chloramphenicol, clindamycin,spectinomycin, polymyxin B, colistin, vancomycin, bacitracin, RP 59500,glycylcyclines and the like.

“Macrolides” means erythromycin, clarithromycin, azithromycin and thelike.

“Anti-tuberculosis drugs” means isoniazid, rifampin, ethambutol,streptomycin, pyrazinamide, ethionamide, aminosalicylic acid,cycloserine, capreomycin and the like.

By drugs for the “anti-Mycobacterium avium agents” we mean rifabutin,macrolides, quinolones, clofazimine, amikacin and the like.

“Anti-leprosy agents” means sulfones such as dapsone and sulfoxonesodium, rifampin, clofazimine, thalidomide and ethionamide.

“Antifungal agents” means systemic antifungal agents such asamphotericin B, flucytosine, imidazoles and triazoles, ketoconazole,miconazole, itraconzole, fluconazole and the like. This category alsoincludes griseofulvin. We also mean topical antifungal agents such asclotrimazole, econazole, miconazole, terconazole, butoconazole,ciclopirox olamine, haloprogin, tolnaftate, naftifine, terbinafine aswell as nystatin, amphotericin B, undecylenic acid, benzoic acid,salicyclic acid, propionic acid, caprylic acid and potassium iodide.

“Antiviral agents” means anti-herpes virus agents such as acyclovir,famciclovir, foscarnet, ganciclovir, idoxuridine, sorivudine,trifluridine, valacyclovir, vidarabine, penciclovir as well as neweragents such as anti HIV-1 such as lamivudine, FTC, adefovir (PMEA),nevirapine, delavirdine, loviride, saquinavir, indinavir, and the like;anti-hepatitis B virus agents such as lamivudine, famciclovir andfialuridine; anti-herpes viruses such as cidofovir (HPMPC) andlobucavir; anti papillomavirus agents such as afovirsen; anti rhinovirusagents such as sICAM-1, pirodavir, and the like; anti-influenza virusdrugs such as GG167; anti-retroviral agents such as didanosine,stavudine, zalcitabine, zidovudine and the like as well as otherantiviral agents such amantadine, interferon alpha, ribavirin andrimantadine.

In accordance with the present invention, the applicants have identifiedan analog of an extracellular signaling factor produced by severalstrains of pathogenic bacteria, including Salmonella typhimurium andEscherichia coli, that affects the pathogenesis or virulence of thesebacteria. They have also identified and cloned genes involved in thebiosynthesis of the naturally-occurring signaling factor. Theidentification of an autoinducer-2 analog and the cloning the genes thatencode proteins involved in biosynthesis of the naturally-occurringautoinducer-2 open a new avenue for drug design aimed at affectingquorum sensing in bacteria. Drugs designed to interfere with quorumsensing constitute a new class of antibiotics. The invention furtherprovides methods for detecting an autoinducer and methods for producingin vitro compounds with autoinducer-2 activity.

Preparation of the Factor with AI-2 Signaling Activity

Initial strategies for purifying the signaling molecule of the inventionresulted in a partially purified preparation comprising the moleculewith a specific signaling activity estimated at about 0.1-1.0 mg of thepartially purified material stimulating a 1,000-fold increase inluminescence, as measured in the V. harveyi bioassay. The signalingactivity does not extract quantitatively into organic solvents and itdoes not bind to either a cation or an anion exchange column. Themolecule is a small (less than 1,000 kDa), polar but uncharged organicfactor. The activity is acid stable and base labile, and it is heatresistant to 80° C. but not 100° C. These features of the signalingmolecule make it clear that the molecule is different from anypreviously described autoinducer.

The signaling factor of the present invention may be purified from itsnatural sources, i.e., the bacteria that produce it. Alterations in theculture medium, e.g., by addition of glucose or another sugar, anincrease in the osmolarity, and/or decreases in pH, can increaseproduction of the signaling molecule in Salmonella and other entericbacteria and have enabled purification of the signaling molecule tonear-homogeneity. Thus, the molecule has now been highly purified fromculture fluids of enteric bacteria (e.g., E. coli, S. typhimurium)through use of the following protocol:

Grow a culture of the signal producing enteric bacterium overnight in LBcontaining 0.5% glucose or another sugar (37° C., with aeration).Inoculate fresh LB containing glucose or another sugar at 0.5% with theovernight culture, at a 1:100 dilution. Grow the diluted culture tomid-exponential phase (3.5 h, 37° C., with aeration).

Pellet the cells (10,000 rpm, 10 min, 4° C.). Discard the culturemedium. Resuspend the cells and wash in {fraction (1/10)}th the originalvolume of low osmolarity NaCl solution (0.1M NaCl in water).

Pellet the cells again (10,000 rpm, 10 min, 4° C.). Discard the lowosmolarity culture fluid. Resuspend the cells in {fraction (1/10)}th theoriginal volume of high osmolarity NaCl solution (0.4 M NaCl in water).Incubate the suspension at 37° C. for 2 h with aeration. During thistime, increased production and secretion of the signaling moleculeoccurs.

Pellet the cells (10,000 rpm, 10 min, 4° C.). Collect the supernatantcontaining the secreted signaling molecule, and filter the supernatantthrough a 0.2 M bacterial filter to remove any remaining cells.

Evaporate the aqueous filtrate using a rotary evaporator at 30° C.Extract the dried filtrate in {fraction (1/10)}th the original volume ofchloroform:methanol (70:30).

Evaporate the organic extract using a rotary evaporator at roomtemperature. Re-dissolve the dried extract in methanol at {fraction(1/100)}th of the original volume.

Subject the partially purified signal to high performance liquidchromatography (HPLC), using a preparative reverse phase C18 column.Elute the molecule with a linear gradient of 0-100% acetonitrile inwater at 5 mL per minute. Collect 30 fractions, 5 mL each.

Assay the HPLC fractions in the V. harveyi BB170 AI-2 assay, and poolthe active fractions.

The product from the C₁₈ column contains the signaling molecule and asmall number of other organic molecules. This purified preparation ofthe signaling molecule has activity 50-100 times greater than that ofthe partially purified material described above (the preparation ofwhich did not include the high osmoticum step or the final HPLC step),i.e., 1-10 μg material stimulates a 1,000-fold increase in luminescencein the V. harveyi bioassay.

Subsequent strategies for purifying the AI-2 analog have led to theidentification of a novel in vitro system for producing AI-2. Thus, inaddition to providing a cloned, overexpressed and purified S.typhimurium LuxS protein, the present invention also provides a methodfor producing AI-2 in vitro. The present invention provides a mechanismfor generating large quantities of pure AI-2 useful for mass spectraland NMR analysis, and for screening compounds that regulate the activityof AI-2. Moreover, the present invention provides a method fordetermining the in vivo biosynthetic pathway for AI-2 synthesis. The invitro method for AI-2 analog production is described below in Example 5and FIG. 15. The method provides a novel means for efficiently producingautoinducer molecules for further study. The method also provides ameans for producing substantial quantities of AI-2 analogs for use incommercial applications. Such applications include, but are not limitedto, adding AI-2 analogs to a growth medium to increase bacterial growth.Such a method is particularly useful in the in the production ofantibiotics from cultured bacteria. Preferably, the AI-2 analog isproduced by the in vitro method set forth in Example 5 of thedisclosure.

Uses of AI-2 Analogs

The autoinducer-2 analogs described here are useful for influencingquorum sensing in bacteria. Such analogs may be identified bylarge-scale screening of a variety of test compounds through use of theV. harveyi bioassay. Reduction in signaling activity in the presence ofa test compound indicates the ability of that compound to, for example,block bacterial pathogenesis by affecting the expression of one or morevirulence factors.

For example, naturally produced compounds can be screened for theireffect on the interaction between autoinducer-2 and receptors for it,such as LuxP and LuxP-LuxQ.

Now that components of the quorum sensing pathway have been identifiedin E. coli, inhibition of one or more of those components can be used toscreen potential signaling molecule inhibitors or analogs. The inventorshave prepared a ler-lacZ reporter fusion construct to be used in testingfor reduction of expression of the Type III secretion gene in E. coliO157:H7 (pathogenic strain) directly. Furthermore, a similar locusexists in S. typhimurium.

Thus, the invention provides a method for selecting autoinducer-2analogs such as 4-hydroxy-5-methyl-2h-furan-3-one by measuring theactivity of a selected gene by the naturally-occurring autoinducer-2 inthe presence and absence of a suspected inhibitor or synergist. In thismanner, compounds that regulate bacterial pathogenesis can be rapidlyscreened.

Compounds identified in the method of the invention can be furtherevaluated, detected, cloned, sequenced, and the like, either in solutionor after binding to a solid support, by any method usually applied tothe detection of a specific DNA sequence such as PCR, oligomerrestriction (Saiki et al., Bio/Technology, 3:1008-1012, 1985),allele-specific oligonucleotide (ASO) probe analysis (Conner et al.,Proc. Natl. Acad. Sci. USA, 80:278, 1983), oligonucleotide ligationassays (OLAs) (Landegren et al., Science, 241:1077, 1988), and the like.Molecular techniques for DNA analysis have been reviewed (Landegren etal., Science, 242:229-237, 1988). Also included in the screening methodof the invention are combinatorial chemistry methods for identifyingchemical compounds that bind to LuxP or LuxQ. See, for example, Plunkettand Ellman, “Combinatorial Chemistry and New Drugs,” ScientificAmerican, April, p.69 (1997).

Naturally-occurring autoinducer-2 can be purified from the native sourceusing conventional purification techniques, derived synthetically bychemical means, or preferably, produced by the in vitro method of theinvention described below.

One of the instant methods entails regulating the activity of anautoinducer-2 receptor comprising contacting an autoinducer-2 receptorwith an AI-2 agonist or antagonist. A further embodiment of this methodemploys a compound of Formulas I, II, III, or IV of any combinationthereof. A further embodiment of either of these embodiments entailswhen the autoinduced-2 receptor is selected from the group consisting ofLux P and Lux Q. Further embodiments of any of the foregoing embodimentsoccur when the AI-2 receptor is found on a bacterial cell, and in turnwhen the bacterial cell is found in a warm-blooded host.

The activity regulated in any of the foregoing embodiments can be, forexample, bacterial cell growth, bacterial virulence, siderophoreexpression, exopolysaccharide production in bacterial cells, bacteriacolony morphology (including smooth colony morphology, such as thatexhibited by a pathogenic bacterial cell), biofilm formation, and thelike. These embodiments can be practiced with compounds from Formulas I,II, III, and IV, or any combination thereof, and especially so with4-hydroxy-5-methyl-3(2H)furanone. One embodiment of any of the foregoingembodiments can be practiced wherein AI-2 receptor is part of abacterial cell selected from the group consisting of Vibrio harveyi,Vibrio cholerae, Vibrio parahaemolyticus, Vibrio alginolyticus,Pseudomonas phosphoreum, Yersinia enterocolitica, Escherichia coli,Salmonella typhimurium, Haemophilus influenzae, Helicobacter pylori,Bacillus subtilis, Borrelia burgfdorferi, Neisseria meningitidis,Neisseria gonorrhoeae, Yersinia pestis, Campylobacter jejuni,Deinococcus radiodurans, Mycobacterium tuberculosis, Enterococcusfaecalis, Streptococcus pneumoniae, Streptococcus pyogenes andStaphylococcus aureus.

The invention further provides methods of inhibiting the infectivity ofa pathogenic organism as well as therapeutic compositions containing anAI-2 analog or AI-2 inhibitor of the invention. The methods compriseadministering to a subject a therapeutically effective amount of apharmaceutical composition that inhibits the activity ofnaturally-occurring AI-2.

A pharmaceutical composition of the invention can include a compound asset forth in Structure I, II, III or IV. A composition including such acompound can, for example, prevent the transcriptional activation ofextracellular virulence factors such as accessory cholera enterotoxin,adenylate cyclase toxin, adhesin, aerolysin toxin, aggregationsubstance, i.e., asa373, Agr A,B,C,D, SigB etc, alkaline protease, alphatoxin, alpha-haemolysin, alveolysin, anthrax toxin, APX toxin, betatoxin, botulinum toxin, bundle forming pilus structural subunit, C2toxin, C3 toxin, C5A peptidase, cardiotoxin, chemotaxis, cholera toxin,ciliotoxin, clostridial cytotoxin, clostridial neutotoxin, collagenadhesion gene, crystal endotoxin, cyaA toxin, cytolysin, delta toxin,delta toxin, delta-lysin, diphtheria toxin, emetic toxin, endotoxin,staphylococcal enterotoxins A, B, C1, C2, C3, D, E, G , enterotoxin,exfoliative toxin, exotoxin, exotoxin A, exotoxin B, exotoxin C,extracellular elastase, fibrinogen, fibronectin binding protein, i.e.,fnbA, filamentous hemagglutinin, fimbriae, gamma hemolysin, gelatinase,i.e., gelE, haemolysin, hemolysin B, hemagglutinin, histolyticolysin,IGG binding protein A, i.e., spaI, intimin, invasin, iron siderophores,ivanolysin, ivanolysin O, lantibiotic modifying enzyme, lantibioticstructural protein, lecithinase, ler (positive regulator of LEE genes),leukotoxin, lipoprotein signal peptidase, listeriolysin O, M protein,motility, neurotoxin, nonfimbrial adhesins, oedema factor,perfringolysin O, permease, pertussis toxin, phospholipase, pili,plasmid encoded regulator per, pneumolysin, poly-D-glutamic acidcapsule, pore-forming toxin, proline permease, RNAIII, RTX toxin, serineprotease, shiga toxin, siderophore/iron acquisition protein, SigAproteases, Spe A, Spe B, Spe C, Sta toxin, Stb toxin, streptolysin O,streptolysin S, superantigen, superoxide dismutase, TCP, tetanus toxin,thiol-activated cytolysin, tracheal cytotoxin, TSST toxin (TSST-1),urease and zona occludens toxin.

The invention provides autoinducer-2 analogs that influence bacterialcell growth or the expression of a bacterial virulence factor byregulating the activity of pathways activated by naturally-occurringautoinducer-2. Such pathways include, for example, the production ofsiderophores and the regulation of bacterial colony morphology. Anautoinducer-2 analog of the present invention can be used to increasebacterial growth by acting in concert with, or as a replacement for,AI-2. Alternatively, an autoinducer-2 analog can inhibit AI-2 bycompeting with naturally-occurring AI-2 for binding to autoinducer-2receptors including LuxP or LuxQ.

In addition, autoinducer-2 receptors such as LuxP or LuxQ provide acommon target for the development of a vaccine. Antibodies raised toautoinducer-2 receptors, such as LuxP or LuxQ, for example, can inhibitthe activation of bacterial pathways associated with virulence.Autoinducer-2 receptors provide common antigenic determinants that canbe used to immunize a subject against multiple pathogen-associateddisease states. Challenging a subject with a polypeptide derived from anautoinducer-2 receptor, or an antigenic fragment thereof, isolated froma particular organism may confer protective immunity to other diseasestates associated with a different organism. For example, a vaccinedeveloped to the LuxP protein isolated from V. cholerae may be capableof cross-reacting with a LuxP homologue expressed by a differentorganism. Thus methods of the present invention can be used to treatpathogen-associated disease states.

The invention further provides a method for promoting production of abacterial product, such as an antibiotic or virulence factor, by addingan autoinducer-2 analog to a culture of bacteria at a concentrationeffective to promote cellular metabolism, growth or recovery. Forexample, antibiotic-producing bacteria typically only produce anantibiotic near the peak of log phase growth. Addition of autoinducer-2analogs to a culture of such bacteria provides a method for inducingantibiotic production at an earlier phase of growth, and/or forincreasing the amount of antibiotic produced.

The invention further provides a method for identifying factors thatdegrade or inhibit synthesis autoinducer-2. The concentration ofnaturally-occurring autoinducer-2 reaches a maximum in early log phaseof bacterial cell growth and subsequently decreases in late log phaseand stationary phase. These data indicate that a mechanism exists forthe degradation of autoinducer-2 at a specific point in bacterialgrowth. The invention enables identification of the mechanism thatcontrols levels of naturally-occurring autoinducer-2. For example,partially purified bacterial extracts can be assayed against isolatedautoinducer-2 to identify those fractions that degrade autoinducer-2.

Autoinducer-2 analogs can also be used in screens for other targets thatthey regulate. Cloned promoter-fusion libraries can be prepared from anyspecies of bacteria and these libraries can be used to identify genesthat are affected by the signaling factor, simply by screening fordifferences in reporter activity in the presence and absence of anautoinducer-2 analog.

Description of Nucleic Acids Encoding Proteins Involved in SignalingFactor Biosynthesis

The applicants have cloned and characterized the genes that encode anovel family of proteins responsible for autoinducer production in V.harveyi, S. typhimurium and E. coli. Members of this family ofautoinducer production genes are designated as luxS, specificallyluxS_(V.h.), luxS_(S.t.), and luxS_(E.c.), for E. coli, V. harveyi, S.typhimurium and E. coli, respectively, and their sequences appear as SEQID NO:1, SEQ ID NO:2 and SEQ ID NOS:3 and 4, respectively (the sequencesread in the 5′ to 3′ direction). Corresponding amino acid sequencesappear as SEQ ID NO:10, SEQ ID NO:11 and SEQ ID NO:12, respectively (andin FIG. 12). It is believed that SEQ ID NOS:1 and 2 constitutefull-length clones, whereas SEQ ID NO:3 and SEQ ID NO:4 do not.

This invention encompasses luxS genes and their encoded enzymes from anybacterial species, having the sequence, structural and functionalproperties of the luxS− encoded proteins described herein. As mentionedin Example 3, homologous nucleic acid sequences have been identified ina variety of bacterial species, but their identity as luxS genesheretofore had not been appreciated. luxS nucleotide and deduced aminoacid sequences from other bacterial species appear as SEQ ID NOS: 5-9and 13-17, respectively, and include sequences from Haemophilusinfluenzae, Helicobacter pylori, Bacillus subtilis, Borrelia burgdorferiand Vibrio cholerae.

Variants and natural mutants of SEQ ID NOS:1-9 are likely to existwithin different species or strains of Vibrio, Escherichia andSalmonella (indeed, E. coli strain DH5α possesses a non-functionalmutant form of the gene). Because such variants are expected to differin nucleotide and amino acid sequence, this invention provides anisolated luxS nucleic acid and encoded protein having at least about50-60% (preferably 60-80%, most preferably over 80%) sequence homologyin the coding region with the nucleotide sequences set forth as SEQ IDNOS:1-9, respectively (and, preferably, specifically comprising thecoding regions of SEQ ID NOS:1-9), and the amino acid sequence of SEQ IDNOS:10-17. Because of the natural sequence variation likely to existamong these proteins and nucleic acids encoding them, one skilled in theart would expect to find up to about 40-50% sequence variation, whilestill maintaining the unique properties of the LuxS-encoded proteins ofthe present invention. Such an expectation is due in part to thedegeneracy of the genetic code, as well as to the known evolutionarysuccess of conservative amino acid sequence variations, which do notappreciably alter the nature of the protein. Accordingly, such variantsare considered substantially the same as one another and are includedwithin the scope of the present invention.

The luxS genes identified here bear no homology to other genes known tobe involved in production of acyl-homoserine lactone autoinducers(luxI-like (Fuqua et al., J. Bacteriol. 176, 269-275, 1994),luxLM-ainS-like (Bassler et al, 1993, supra; Gilson et al, J. Bacteriol.177, 6946-6951, 1995). Database analysis of bacterial genomes revealsthat many other species of bacteria possess a gene homologous to luxSfrom V. harveyi, S. typhimurium and E. coli, as shown in Table 1.

TABLE 1 percent homology percent identity to LuxS of to LuxS ofbacterium V. harveyi V. harveyi Haemophilus influenza 88 72 Helicobacterpylori 62 40 Bacillus subtilis 58 38 Borrelia burgfdorferi 52 32Neisseria meningitidis 89 80 Neisseria gonorrhoeae 89 80 Yersinia pestis85 77 Campylobacter jejuni 85 74 Vibrio cholerae 95 90 Deinococcusradiodurans 65 45 Mycobacterium tuberculosis 59 41 Enterococcus faecalis60 44 Streptococcus pneumoniae 57 36 Streptococcus pyogenes 57  36.

Mutagenesis of luxS in V. harveyi, S. typhimurium and E. coli eliminatesproduction of the signaling molecule in all three species of bacteria.S. typhimurium could be complemented to full production of the moleculeby the introduction of either the E. coli O157:H7 luxS_(E.c.) gene orthe V. harveyi BB120 luxS_(V.h.) gene. These results indicate that boththe E. coli and V. harveyi LuxS proteins can function with S.typhimurium cellular components to produce the signaling molecule.Introduction of either the E. coli O157:H7 luxS_(E.c.) or the V. harveyiBB120 luxS_(V.h.) gene partially complemented E. coli DH5α to producenaturally-occurring autoinducer-2.

Pathogenicity is connected with quorum sensing. Pathogenic andnon-pathogenic strains differ in their production of naturally-occurringautoinducer-2. For example, E. coli O157:H7 strains producenaturally-occurring autoinducer-2 with or without glucose while E. coliK-12 strains do not produce it in the absence of a preferred carbonsource. Furthermore, all of the E. coli O157 strains tested producegreater signaling activity than do non-pathogenic E. coli strains.Similarly, pathogenic S. typhimurium 14028 produces significantly moresignaling activity than does S. typhimurium LT2.

Preparation of LuxS Nucleic Acids, Encoded Proteins, and ImmunologicallySpecific Antibodies

Nucleic Acids

Nucleotide sequence information, such as the DNAs having SEQ ID NOS:1-9,enables preparation of an isolated nucleic acid molecule of theinvention by oligonucleotide synthesis. Synthetic oligonucleotides maybe prepared by the phosphoramadite method employed in the AppliedBiosystems 38A DNA Synthesizer or similar devices. The resultantconstruct may be purified according to methods known in the art, such ashigh performance liquid chromatography (HPLC). Long, double-strandedpolynucleotides, such as a DNA molecule of the present invention, mustbe synthesized in stages, due to the size limitations inherent incurrent oligonucleotide synthetic methods. Such long double-strandedmolecules may be synthesized as several smaller segments of appropriatecomplementarity. Complementary segments thus produced may be annealedsuch that each segment possesses appropriate cohesive termini forattachment of an adjacent segment. Adjacent segments may be ligated byannealing cohesive termini in the presence of DNA ligase to construct anentire 1.8 kb double-stranded molecule. A synthetic DNA molecule soconstructed may then be cloned and amplified in an appropriate vector.

LuxS nucleic acids also may be isolated from appropriate biologicalsources through use of known methods. In a preferred embodiment, agenomic clone is isolated from a cosmid expression library of an S.typhimurium or E. coli genome, or a genomic clone is isolated from acosmid library of another bacterial genome.

Nucleic acids having the appropriate level sequence homology with theprotein coding region of any of SEQ ID NOS:1-9 may be identified by useof hybridization and washing conditions of appropriate stringency. Forexample, hybridizations may be performed, according to the method ofSambrook et al., through use of hybridization solution comprising:5×SSC, 5×Denhardt's reagent, 1.0% SDS, 100 g/ml denatured, fragmentedsalmon sperm DNA, 0.05% sodium pyrophosphate and up to 50% formamide.After hybridization at 37-42° C. for at least six hours, filters arewashed as follows: (1) five minutes at room temperature in 2×SSC and 1%SDS; (2) fifteen minutes at room temperature in 2×SSC and 0.1% SDS; (3)thirty minutes to one hour at 37° C. in 1×SSC and 1% SDS; (4) 2 hours at42-65° in 1×SSC and 1% SDS, changing the solution every 30 minutes.

LuxS nucleic acids can also be found through a search of publiclyavailable databases for the luxS sequence in the bacterial genome ofinterest, design of PCR primers from the sequence, amplification of thegene directly from the chromosome, and cloning of the PCR product.Alternatively, if the complete sequence of a specific bacterial genomeis not available, the sequences set forth in the present invention, orany other luxS sequence, may be used to design degenerateoligonucleotides for PCR amplification and cloning of luxS from thechromosome.

Nucleic acids of the present invention may be maintained as DNA in anyconvenient cloning vector. In a preferred embodiment, clones aremaintained in plasmid cloning/expression vector, such as pBluescript(Stratagene, La Jolla, Calif.), which is propagated in a suitable E.coli host cell.

LuxS nucleic acids of the invention include DNA, RNA, and fragmentsthereof, which may be single or double-stranded. Thus, this inventionprovides oligonucleotides (sense or antisense strands of DNA or RNA)having sequences capable of hybridizing with at least one sequence of anucleic acid molecule of the present invention, such as selectedsegments of the DNA having SEQ ID NOS:1, 2 or 3. Such oligonucleotidesare useful as probes for detecting luxS genes or transcripts.

Proteins and Antibodies

A full-length luxS gene product of the present invention may be preparedin a variety of ways, according to known methods. The protein may bepurified from appropriate sources, e.g., cultured bacteria such as S.typhimurium, E. coli or V. harveyi.

The availability of full-length luxS nucleic acids enables production ofthe encoded protein through use of in vitro expression methods known inthe art. According to a preferred embodiment, the enzyme may be producedby expression in a suitable expression system. For example, part or allof a DNA molecule, such as the DNA having SEQ ID NO:1 or 2, may beinserted into a plasmid vector adapted for expression in a bacterialcell, such as E. coli, or a eucaryotic cell, such as Saccharomycescerevisiae or other yeast. Such vectors comprise the regulatory elementsnecessary for expression of the DNA in the host cell, positioned in sucha manner as to permit expression of the DNA in the host cell. Suchregulatory elements required for expression include promoter sequences,transcription initiation sequences and, optionally, enhancer sequences.

The protein produced by luxS gene expression in a recombinantprocaryotic or eucyarotic system may be purified according to methodsknown in the art. In a preferred embodiment, a commercially availableexpression/secretion system can be used, whereby the recombinant proteinis expressed and thereafter secreted from the host cell, to be easilypurified from the surrounding medium. If expression/secretion vectorsare not used, an alternative approach involves purifying the recombinantprotein by affinity separation, such as by immunological interactionwith antibodies that bind specifically to the recombinant protein. Suchmethods are commonly used by skilled practitioners.

The protein encoded by the luxS gene of the invention, prepared by oneof the aforementioned methods, may be analyzed according to standardprocedures. For example, the protein may be subjected to amino acidsequence analysis, according to known methods. The stability andbiological activity of the enzyme may be determined according tostandard methods, such as by the ability of the protein to catalyzeproduction of the signaling molecule under different conditions.

The present invention also provides antibodies capable ofimmunospecifically binding to the luxS-encoded protein of the invention.

Uses of LuxS Nucleic Acids, Encoded Protein and Immunologically SpecificAntibodies

LuxS nucleic acids or fragments thereof may be used as probes for luxSgenes in (1) in situ hybridization; (2) Southern hybridization (3)northern hybridization; and (4) assorted amplification reactions such aspolymerase chain reactions (PCR). They may also be used as probes toidentify related genes from other bacteria.

LuxS nucleic acids may further be used to produce large quantities ofsubstantially pure encoded protein, or selected portions thereof.Furthermore, the cloned genes inserted into expression vectors can beused to make large quantities of the signaling molecule itself, from anyselected bacterial species, in a recombinant host such as E. coli DH5α.Cloning of specific luxS genes, and production of a large quantity ofthe encoded protein, thereby allows production of a large quantity ofthe specific autoinducer. This capability will be particularly useful indetermining differences, if any, in the structures of autoinducers fromdifferent species. Alternatively, large quantities of signaling moleculefrom the species of interest could be made through use of the clonedgene in an expression vector, and thereafter used in library screens forpotential targets in Petri plate assays.

Purified luxS gene products, or fragments thereof, may be used toproduce antibodies that also may serve as sensitive detection reagentsfor those proteins in cultured cells. Recombinant techniques enableexpression of fusion proteins containing part or all of a selectedluxS-encoded protein. The full length protein or fragments of theprotein may be used to advantage to generate an array of antibodiesspecific for various epitopes of the protein, thereby providing evengreater sensitivity for detection of the protein. Other uses of the LuxSproteins include overproduction to make a quantity sufficient forcrystallization. Knowledge of the crystal structure of the LuxS proteinswould enable determination of the LuxS active site that produces thenaturally-occurring autoinducer-2, and that could therefore be used forcomputer-aided design of autoinducer-2 analogs, LuxS inhibitors, andrational drug design.

Antibodies specific for a LuxS-encoded protein may be used in a varietyof assays designed to detect and quantitate the protein. Such assaysinclude, but are not limited to: (1) flow cytometric analysis; (2)immunochemical localization of a LuxS protein in cells or tissues; and(3) immunoblot analysis (e.g., dot blot, Western blot) of extracts fromvarious cells and tissues. Additionally, as described above, antibodiescan be used for purification of the proteins (e.g., affinity columnpurification, immunoprecipitation).

Vibrio Harveyi Screening Strain

The invention provides a luxN− and luxS− strain of V. harveyi,designated MM32, for identifying inhibitors of the quorum-sensingpathway. Since the new strain is luxN− (i.e., sensor 1−), AI-1 does notaffect its ability to grow or to luminesce. Further, since MM32 cannotproduce AI-2, addition of exogenous AI-2 or its analogs allows rapididentification of inhibitors of AI-2.

V. harveyi strains containing separate mutations in Lux genes L or M, orin Lux genes S or Q, lack the ability to synthesize or detectautoinducer-1 or autoinducer-2, respectively. Use of strain BB170, whichis sensor 1−, sensor 2+ (LuxN−, LuxQ+) allows detection of autoinducer-2in diverse bacteria. The light emission response of wild type, LuxN− andLuxQ− phenotypes to increasing cell density is shown in FIG. 14.

The strains described above are ideally suited for the preparation of akit. Such a kit may comprise a carrier compartmentalized to receive oneor more containers such as vials, tubes, and the like, each of thecontainers comprising one of the separate elements to be used in themethod. The container may comprise a strain of bacteria capable ofdetecting the presence of an autoinducer. Preferably, the bacterialstrain is capable of providing a signal in the presence ofautoinducer-2. More preferably, the desired strain lacks the ability todetect AI-1 (sensor 1−) and to synthesize AI-2. Thus, the kit mayprovide a luxN− and luxS− strain of V. harveyi designated MM32 foridentifying autoinducer-2 as well as inhibitors of autoinducer-2 and thequorum-sensing pathway.

Methods for Detecting a Bacterial Biomarker

The present invention provides methods of using autoinducer-2 analogs toidentify and regulate the expression of bacterial biomarkers inbacteria. The method is particularly useful for identifying a biomarkerof pathogenic bacteria, which are thought to express an antigenicdeterminant or other biomarker in response to increased autoinducerconcentration in the surrounding environment. Thus the present inventionprovides a method for identifying such a biomarker by exposing abacterium to an autoinducer-2 analog and assaying for the presence ofthe biomarker through use of a labeled nucleic acid or otherbiomolecule, such as an antibody.

The method can be used in a screen to detect infections, for example. Inaddition, the method of the invention can be used to analyzedifferential gene expression in a bacterial cell following contact withan autoinducer through comparison of the expression of genes indifferent cells.

The materials described above are ideally suited for the preparation ofa kit. Such a kit may comprise a carrier compartmentalized to receiveone or more containers such as vials, tubes, and the like, eachcontainer comprising one of the separate elements to be used in themethod. A kit of the invention may contain a first container comprisingisolated autoinducer-2. The isolated autoinducer-2 can be used toregulate the expression of a biomarker in a target bacterium. Forexample, autoinducer-2 can be used to induce expression of a particularbiomarker that can then be identified by a probe. Thus, the kit maycontain a second container comprising a probe that can be detectablylabeled. The kit may also have a third container comprising a reporter,such as a biotin-binding protein, such as avidin or streptavidin, boundto a label, such as an enzymatic, fluorescent, or radionuclide label.Other reporters and labels are well known in the art. For example, thekit of the invention may provide reagents necessary to perform nucleicacid hybridization analysis as described herein or reagents necessary todetect antibody binding to a target.

Regulation of Biofilm Formation

Bacteria can adhere to solid surfaces to form slimy, slippery coatingsknown as biofilms, which are a highly hydrated matrix of exopolymers,typically polysaccharide, and other biopolymers. The biofilm mode ofexistence, involving colony-forming sessile bacteria, accounts for asizable portion of the biomass in many environments. In some instances,biofilm-associated forms of bacteria may outnumber their planktonic(free-swimming) equivalents by several orders of magnitude. Thetransition from a planktonic existence to growth attached to a surfaceoccurs in response to many environmental factors, including long-termgrowth under conditions of nutrient deprivation or high osmolarity.Biofilms may contain either a single species, or multiple species ofbacteria, and these can be organized into higher order structures (e.g.water/nutrient channels, cellular pillars, dense monolayers punctuatedby microcolonies) that benefit the entire community. Biofilm coloniesexhibit coordinated metabolic responses, such as spatially distinct geneexpression in different regions of the biofilm, that contribute to theiroverall fitness. Biofilms allow bacteria to survive in hostileenvironments.

Bacterial biofilms are at the root of many persistent and chronicbacterial infections. Consequently, the prevention of colonization, anderadication of biofilm-associated bacteria is a major goal of modemmedicine. Unlike single cells, biofilm formation can withstand exposureto most biocidal treatments. In the biofilm, the extracellular matrix(glycocalyx) provides a barrier that protects and isolates themicroorganisms from biocides such as surfactants and antibiotics. In onestudy, biofilm cultures were able to withstand a dose of antibiotictwenty-fold greater than needed to eradicate planktonic cultures of thesame bacteria. It also shields the resident microorganisms from hostdefense mechanisms such as antibodies and antigen processing byphagocytes.

Biofilm-associated infections have been implicated in a number ofdisease conditions. Examples include porstatitis, osteomyelitis, septicarthritis, and cystic fibrosis. In some of these diseases (e.g. septicarthritis), the biofilm can cause destruction of the host surfacestructure. In many of these conditions, the biofilm provides a reservoirof bacteria that can lead to chronic and recurrent infections (sepsis).Biofilm formation can also be a complication in bioimplants, such asbone prostheses, heart valves, and pacemakers. Biofilm formation maycompromise the function of the implant, or lead to serious bone or jointinfections.

Because quorum sensing strongly influences biofilm formation,quorum-sensing blockers can impede formation of biofilms andsubstantially decrease the extent of biofilms that have already formedon a surface. Thus, by providing the structure of autoinducer-2 (AI-2)and analogs of AI-2, such as Structure I, II, III or IV, the presentinvention provides a new approach to inhibiting bacterial infections byregulating biofilm formation.

The invention further provides data indicating that AI-2 regulatesbacterial biofilm formation. Null mutant strains of V. harveyi lackingautoinducer-1 and autoinducer-2 activity (AI-1−/AI-2−) do not producebiofilm, unlike wild type, AI-1−/AI-2+ and AI-1+/AI-2− V. harveyistrains. Addition of AI-1, AI-2 or Salmonella AI-2 to the medium allows(AI-1−/AI-2−) V. harveyi to produce biofilm. Thus, the inventionprovides a way of regulating biofilm formation by contacting a bacterialcell with autoinducer-2 or an autoinducer-2 analog.

Furthermore, the unexpected finding that quorum-sensing blockers inhibitbiofilm formation implies that compounds that exhibit quorum-sensingblocking in other systems, such as protease production, will alsoinhibit biofilm formation.

In another embodiment, the invention provides a method of removing abiofilm from a surface that comprises treating the surface with acompound of the invention. The surface is preferably the inside of anaqueous liquid distribution system, such as a drinking waterdistribution system or a supply line connected to a dental air-watersystem, where removal of biofilms can be particularly difficult toachieve. The compound is preferably applied to the surface either aloneor together with other materials such as conventional detergents orsurfactants.

A further embodiment of the invention is an antibacterial compositioncomprising a compound of the invention together with a bacteriocidalagent. In the antibacterial compositions, the compound of the inventionhelps to remove the biofilm while the bacteriocidal agent kills thebacteria. The antibacterial composition is preferably in the form of asolution or suspension for spraying and/or wiping on a surface.

In yet another aspect, the invention provides an article coated and/orimpregnated with a compound of the invention in order to inhibit and/orprevent biofilm formation thereon. The article is preferably composed ofplastic with the compound of the invention distributed throughout thematerial.

Synergistic Antibiotic Compositions

In a further embodiment, the invention provides a synergistic antibioticcomposition comprising an antibiotic and an inhibitor of thequorum-sensing pathway of a microorganism, or apharmaceutically-acceptable salt thereof, and one or morepharmaceutically acceptable carriers, adjuvants or vehicles.

The synergistic antibiotic composition of the invention can be used totreat infections in a warm-blooded animal caused by microorganismspossessing a quorum-sensing mechanism, which comprises administering tothe animal a therapeutically effective amount of the synergisticantibiotic composition of this invention.

Surprisingly, we have found that combinations of inhibitors for one ormore of the quorum sensing pathways with antibiotics effective againstmicroorganisms containing the quorum sensing mechanism reduces theamount of antibiotic normally necessary for its therapeutic effect.Also, the combination may lower the therapeutically effective amount ofthe antibiotic so that it has a beneficial effect against themicroorganism when ordinarily it was considered to have no effect atconcentrations considered both effective and safe. Thus, another aspectof the instant invention is directed to a synergistic antibioticcomposition comprising an antibiotic and an inhibitor of thequorum-sensing pathway of a microorganism. By “synergistic”, we meanthat the combination of the quorum sensing inhibitor lowers the dose ofthe antibiotic required to kill (in a bactericidal agent) or arrest thegrowth (in a bacteristatic agent) of the microorganism being treated inwarm-blooded animal, or renders the antibiotic effective against theorganism in an animal when it ordinarily is not effective.

By “inhibitor of the quorum-sensing pathway of a micro organism” we meaninhibitors that can either inhibit the production, or the response to,an autoinducer. Such inhibitors may inhibit one or more of the AI-1,AI-2 and the peptide-mediated quorum sensing pathways. For instance,inhibitors of the AI-2 pathway (depicted in FIG. 13) are molecules thateither bind to or inhibit the production of the proteins derived fromthe LuxP, LuxS and LuxQ genes of the V. harveyi and their homologs inother species. The assays for detecting inhibitors of the AI-1 , AI-2and peptide-mediated sensing pathways appear in Examples 6, 4, and 7,respectively. For the AI-2 pathway, inhibitors are found by theirinhibition of bioluminescence of mutant strains V. harveyi that areotherwise insensitive to the effects of AI-1. Inhibitors of the AI-1pathway are also measured by their ability to inhibit bioluminescence ofV. fischeri. Finally, inhibitors of the peptide-mediated quorum sensingpathway are detected by their ability diminish the production of thevirulence factor δ-toxin from Staphlycoccus aureus as colonies of thisbacteria grew to confluence.

Examples of inhibitors of the AI-1 quorum sensing pathway are analogs ofN-acyl-L-homoserine lactones in which the N-acyl side chain has beenmodified, specifically:

A modified N-butyryl-L-homoserine lactone compound of the structure V:

or a modified N-(3-oxododecanoyl)-L-homoserine lactone compound of thestructure VI:

wherein R₁-R₂₂ are independently selected from the group consisting ofC₁ to C₄ alkyl; a hydrogen atom, hydroxy, amino, and thiol;

R₂₂-R₂₃ are independently an oxygen or a sulfur atom; and

R₂₄-R₂₈ are independently a hydrogen or a halogen atom. These moleculesare described in Davies et al., PCT Patent Application Publication No.WO98/58075, published Dec. 23, 1998, the entirety of which isincorporated herein by reference.

Other examples of inhibitors of AI-1 quorum-sensing pathways arehalogenated furanones of the structure VII:

These halogenated furanones are produced by benthic marine macroalga D.pulchra. One particular example of such an inhibitor is4-bromo-5-(bromomethylene)-3-(1-hydroxybutyl)-2-(5H)-furanone. Thesemolecules are described in Manefield et al., Microbiology, 145, 283-291(1999)).

Examples of the inhibitors of the AI-2 mediated quorum sensing pathwayincludes compounds of structures I, II, III and IV:

wherein C² is additionally bonded to at least one substituent selectedfrom hydrogen, hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅ alkanoyl, C₂₋₅alkanoyloxy, heteroaryl, or forms a double bond with an oxygen atom orC³; wherein C³ is additionally bonded to at least one substituentselected from hydrogen, hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅alkanoyl, C₂₋₅ alkanoyloxy, or forms a double bond with an oxygen atomor C²; wherein C⁴ is additionally bonded to at least one substituentselected from hydrogen, C₁₋₅ alkyl, C₂₋₅ alkanoyl, C₂₋₅ alkanoyloxy, orforms a double bond with an oxygen atom or C⁵; and wherein C⁵ isadditionally bonded to at least one substituent selected from hydrogen,C₁₋₅ alkyl, C₂₋₅ alkanoyl, C₂₋₅ alkanoyloxy, or forms a double bond withan oxygen atom or C⁴; wherein at least one of C², C³, C⁴ or C⁵ is bondedto a substituent selected from hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅alkanoyl, and heteroaryl; and wherein at most one carbon-carbondouble-bond is present in the ring of Structure I;

wherein R is a C₁₋₅ alkoxyl group;

wherein X is either an oxygen, sulfur or nitrogen atom; R_(1a) is eitherhydrogen, hydroxy, alkyl, acyl, amido, hydroxyl, amino, thio, or aryl;R_(1b) is either hydrogen, hydroxy, alkyl, acyl, amido, hydroxyl, amino,mercapto, thio, or aryl, or R_(1a) and R_(1b) can include the same atombonded to C₂ to form a double bond with C₂; R₂ is hydrogen, alkyl, orhalogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino, thio, oraryl; R₄ is hydrogen or alkyl, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond;

wherein X is oxygen, sulfur or nitrogen; R_(7a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(7b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(7a) and R_(7b) can together form a double bond; R₆ is hydrogen,alkyl, or halogen; R₇ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₈ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.

Examples of inhibitors of peptide-mediated quorum sensing moleculesinclude chemically-modified pheromones of Staphylococcus epidermidisthat are competent inhibitors of the Staphylococcus aureus agr(accessory gene regulator) system. These inhibitors include molecules ofthe structures VIII and IX:

(cyclo-SVCASYF)

(cyclo-DSV(DAPA)ASYF)

These modified pheromones were especially effective in inhibitingproduction of δ-toxin in the S. aureus strains as described in Otto etal., FEBS Letters, 450 257-262 (1999).

Further inhibitors of peptide-mediated quorum sensing are compounds ofthe structure:

(cyclo)-YSTCDFIM;(X)

(cyclo)-GVNACSSLF;(XI)

(cyclo)-GVNASSSLF; or(XII)

(cyclo)-GVNA(DAPA)SSLF, (XIII)

wherein in the these four structures the C-terminal carbonyl groupforms 1) a thiolactone with the sulfur atom of the cysteine residue(YSTCDFIM and GVNACSSLF); 2) a lactone group with the oxygen atom of thefirst serine residue (GVNASSSLF); or 3) an amide bond with amino groupof the diaminoproprionic acid (DAPA) residue (GVNA(DAPA)SSLF). Thesynthesis of these molecules and activity of these molecules have beendescribed in Mayville et al., Proc. Natl. Acad. Sci. USA, 96, 1218-1223(1999).

Further embodiments of the instant synergistic antibiotic compositioninclude those wherein the inhibitor inhibits the AI-1 quorum sensingpathway. Of this latter embodiment, further specific embodiments includethose where the inhibitor is a halogenated 2(5H) furanone of StructureVII above, or when the inhibitor is either a modifiedN-buturyl-L-homoserine lactone of Structure VIII above or a modifiedN-(3-oxododecanoyl)-L-homoserine lactone of Structure IX above.

Another group of embodiments occurs when the inhibitor of thesynergistic antibiotic composition is one that inhibits the AI-2 quorumsensing pathway, and more so when it is of the Structure III orStructure IV above. One further embodiment is when the inhibitor is2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone. Another group of embodimentsfor a composition containing an AI-2 inhibitor occurs when 1) theantibiotic is a penicillin, and further when the penicillin isampicillin; 2) the antibiotic is a quinoline, and further when thequinoline is ciprofloxacin; 3) the antibiotic is vancomycin; and 4) theantibiotic is a sulfonamide, and further when the sulfonamide issulfisoxaxole.

Synergistic antibiotic compositions where the inhibitor inhibits thepeptide-mediated quorum sensing pathway constitute another embodiment ofthe instant synergistic compositions. Within this latter embodiment arethose compositions that include inhibitors of the Structure (VIII) and(IX) above, and alternatively those that contain inhibitors ofStructures (X) through (XIII) above.

Yet another group of embodiments of the instant synergistic antibioticcompounds occurs when 1) the antibiotic is a penicillin, and furtherwhen the penicillin is ampicillin; 2) the antibiotic is a quinoline, andfurther when the quinoline is ciprofloxacin; 3) the antibiotic isvancomycin; and 4) the antibiotic is a sulfonamide, and further when thesulfonamide is sulfisoxaxole.

Further embodiments of the instant pharmaceutical compositions trackthose set forth above for the synergistic antibiotic compositions ofthis invention, as determined by the identity of the inhibitors andantibiotics in the pharmaceutical composition.

A further aspect of this invention is directed to a method of treatinginfections in a warm-blooded animal caused by microorganisms possessinga quorum-sensing mechanism that comprises administering to the animal atherapeutically effective amount of the synergistic antibioticcomposition of this invention. It will be understood that the amount ofantibiotic administered in the instant method will normally be less thanthat administered if the inhibitor compound were not present. The amountnormally necessary to treat an infection by a particular microorganismcan be determined by using the antibiotic susceptibility assay ofExample 8, and also in the case of known antibiotics by consultingsources such as J. Hardman and L. Limbard, Editors-in-Chief, Goodman andGilman's The Pharmacological Basis of Therapeutics, Ninth Edition,McGraw-Hill, New York, (1996), especially at pages 1027 through 1223. Ofcourse, the synergistic antibiotic composition administered in thismethod can also be in the form of a pharmaceutical composition of thisinvention. Also, the synergistic antibiotic compound can be administeredto warm-blooded animal infected with a microorganism possessing a quorumsensing pathway that would otherwise be refractory to the treatment withthe antibiotic alone if screens such as the one set forth in Example 8below indicate that the synergistic antibiotic composition does indeedhave activity against that microorganism.

Further embodiments of this method includes methods for treatinginfections in warm blooded animals caused by Streptococcus pyogenes, andespecially so when the inhibitor that is administered is one thatinhibits the AI-2 quorum sensing pathway. Of this latter embodiment,further embodiments include those where the antibiotic is vancomycin,when the antibiotic is a quinoline antibiotic, for example,ciprofloxacin; or when the antibiotic is a sulfonamide, for example,sulfisoxazole.

Yet another embodiment of the instant method includes methods fortreating infections in warm blooded animals caused by Staphylococcusaureus, and especially so when the inhibitor inhibits the AI-2quorum-sensing pathway. Of this latter embodiment, further embodimentsinclude those wherein the antibiotic is a penicillin, and in particularwhen the antibiotic is ampicillin.

Medical Devices

In another embodiment, the compounds and synergistic antibioticcompositions of the invention can be used to inhibit bacterial cellgrowth and/or biofilm formation on a medical device. Percutaneousdevices (such as catheters) and implanted medical devices (e.g.,pacemakers, vascular grafts, stents, and heart valves) commonly serve asfoci for bacterial infection. The tendency of some microorganisms toadhere to and colonize the surface of the device promotes suchinfections, which increase the morbidity and mortality associated withuse of the devices. Consequently, physicians have great interest indevelopment of surfaces that are less prone to bacterial colonization.

The synergistic antibiotic compositions of the invention can be used toinhibit bacterial cell growth and biofilm formation on substrates usedto manufacture medical devices associated with noninvasive and invasivemedical procedures. Such substrates include tubular, sheet, rod andarticles of proper shape for use in a number of medical devices such asvascular grafts, aortic grafts, arterial, venous, or vascular tubing,vascular stents, dialysis membranes, tubing or connectors, bloodoxygenator tubing or membranes, surgical instruments, ultrafiltrationmembranes, intra-aortic balloons, stents, blood bags, catheters,sutures, soft or hard tissue prostheses, synthetic prostheses,prosthetic heart valves, tissue adhesives, cardiac pacemaker leads,artificial organs, endotracheal tubes, lenses for the eye such ascontact or intraocular lenses, blood handling equipment, apheresisequipment, diagnostic and monitoring catheters and sensors, biosensors,dental devices, drug delivery systems, or bodily implants of any kind.For example, arthroscopic surgery is routinely performed with use ofmedical devices that minimize the invasiveness of the procedure. Suchdevices include, for example, ultrathin microfiberoptic endoscopes thatoffer the laryngologist unique access to the limited spaces of thetemporal bone and skull base. In another example, a stent supplementedwith a composition of the invention that deters bacterial infectionsresulting from the presence of the implanted stent can be constructed.Stents are used to maintain an open lumen in tissues including thetracheo-bronchial system, the biliary hepatic system, the esophagealbowel system, and the urinary tract system. U.S. Pat. No. 5,637,113issued to Tartaglia, and incorporated herein by reference, teaches astent with a sheet of polymeric film wrapped around the exterior. Withregard to the present invention, the film may be loaded or coated with acompound or composition of the invention. Alternatively, the materialused to manufacture the stent can be impregnated with a composition ofthe invention.

A medical device may be further supplemented with, for example, one ormore antibodies, analgesics, anticoagulants, anti-inflammatorycompounds, antimicrobial compositions, cytokines, drugs, growth factors,interferons, hormones, lipids, demineralized bone or bone morphogeneticproteins, cartilage inducing factors, oligonucleotides polymers,polysaccharides, polypeptides, protease inhibitors, vasoconstrictors orvasodilators, vitamins, minerals, stabilizers and the like.Supplemented, as used herein, includes medical devices that areimpregnated, infused, coated, covered, layered, permeated, attached orconnected with a compound or synergistic antibiotic composition of theinvention. Methods for immobilizing biomaterials to a medical device arediscussed in U.S. Pat. No. 5,925,552, which is incorporated herein byreference. Additional methods of coating surfaces of medical deviceswith antimicrobial compositions are taught in U.S. Pat. No. 4,895,566 (amedical device substrate carrying a negatively charged group having apKa of less than 6 and a cationic antibiotic bound to the negativelycharged group); U.S. Pat. No. 4,917,686 (antibiotics are dissolved in aswelling agent which is absorbed into the matrix of the surface materialof the medical device); U.S. Pat. No. 4,107,121 (constructing themedical device with ionogenic hydrogels, which thereafter absorb orionically bind antibiotics); U.S. Pat. No. 5,013,306 (laminating anantibiotic to a polymeric surface layer of a medical device); and U.S.Pat. No. 4,952,419 (applying a film of silicone oil to the surface of animplant and then contacting the silicone film bearing surface withantibiotic powders). U.S. Pat. No. 5,902,283 further discloses a methodfor coating a medical device with an antimicrobial agent such that theagent penetrates the exposed surfaces of the device and is impregnatedthroughout the material of the device.

The desirability of coating medical devices such as, inter alia,surgical implants, sutures and wound dressings with pharmaceuticalagents is well documented in the art. Such coated devices couldtheoretically provide a means for locally delivering pharmaceutical ortherapeutic agents at the site of medical intervention to treat avariety of diseases. For example, surgical implants or sutures coatedwith antibiotics can provide local delivery of antibiotic directly at animplantation or suture site, thereby decreasing the onset of infectionfollowing the surgical intervention. Thus, compounds and synergisticantibiotic compositions of the invention can supplement medical devicesused for implantation in guided tissue regeneration (GTR) procedures bypreventing or ameliorating infections at the site of tissueregeneration. Such devices and procedures are currently used by thoseskilled in the medical arts to accelerate tissue regeneration followinginvasive surgical procedures. For example, nonresorbable orbioabsorbable membranes are used to accelerate tissue regeneration bypromoting the repopulation of the wound area with cells that form thearchitectural and structural matrix of the tissue. The compounds andsyngeristic antibiotic compositions of the invention can be used toinhibit bacterial growth at the site of tissue regeneration. Forexample, a compound or syngeristic antibiotic composition can be used toaid periodontal tissue regeneration in a human or lower animal byplacing a composition containing a bioresorbable polymer, leachablesolvent, and a compound or syngeristic composition of the invention, ata site in need of periodontal tissue regeneration in a human or othermammal such that the composition is effective for inhibiting bacterialcell growth by releasing a therapeutically-effective amount of thecompound or syngeristic composition at the site.

A medical device supplemented with a compound or composition of theinvention is further useful for promoting tissue growth during theprocess of tissue engineering. By “tissue engineering” is meant thecreation, design, and fabrication of biological prosthetic devices, incombination with synthetic or natural materials, for the creation,augmentation, or replacement of body tissues and organs. Thus, a medicaldevice supplemented with a compound or composition of the inventionincludes cell-containing or cell-free device that induce theregeneration of functional human tissues when implanted at a site thatrequires regeneration. As previously discussed, biomaterial-guidedtissue regeneration can be used to promote cell proliferation in, forexample, digestive tract tissue for treatment of gastric ulcers or thepathogenic result of Crohn's disease. A compound or synergisticantibiotic composition of the invention can be used to promote thegrowth of reconstituted tissues assembled into three-dimensionalconfigurations at the site of a wound or other tissue in need of suchrepair by inhibiting pathogenic bacterial cell growth at the site. Acompound or synergistic antibiotic composition can be included with thedevice upon implantation or the device itself can be impregnated with acompound or synergistic antibiotic composition such that the compound orsynergistic antibiotic composition is released slowly during tissueregeneration.

A compound or synergistic antibiotic composition of the invention can beincluded in external or internal medical devices containing humantissues designed to replace the function of diseased internal tissues.This approach involves isolating cells from the body, placing them on orwithin structural matrices, and implanting the new system inside thebody or using the system outside the body. A compound or synergisticantibiotic composition invention can be included in such matrices topromote the growth of tissues contained in the matrices by inhibitingbacterial growth. For example, compound or synergistic antibioticcomposition of the invention can be included in a cell-lined vasculargraft to inhibit bacterial cell growth and biofilm formation in thegraft. It is envisioned that the invention can be used to augment tissuerepair, regeneration, and engineering in products, such as epithelialtissue, cartilage and bone, central nervous system tissues, muscle,liver, and pancreatic islet (insulin-producing) cells.

A specific, non-limiting example is the use of the invention inpromoting the growth of skin graft replacements that are used as atherapy in the treatment of burns and ulcers. Burn victims areparticularly susceptible to infections resulting from skin grafttreatments. The compounds or synergistic antibiotic composition of theinvention can be included during tissue engineering of a skin graft suchthat the graft is free of bacterial infection when transplanted to aburn victim. Compounds or synergistic antibiotic compositions of theinvention can also be included at the site of transplant to furtherminimize the possibility of infection. Thus, the invention encompassesinhibiting bacterial cell growth and biofilm formation duringpreparation and application of a tissue graft using an effective amountof a compound or synergistic antibiotic composition of the invention.

Additionally, or alternatively, the synergistic antibiotic compositionsof the invention may be incorporated into a biodegradable carrier. Forexample, such a carrier is described in U.S. Pat. No. 5,788,979.Time-controlled release of the compound or composition is attributableto the degradation or disintegration of the carrier itself, so that thedrug or other agent remains captive within the carrier until it isdispensed or released, i.e., freed from its host, by progressivedissolution upon continuing diffusion of the carrier from the reservoir.The compound or composition tends to act locally rather thansystemically in such an arrangement.

It is further envisioned that the synergistic antibiotic compositions ofthe invention can be used to aid wound repair. For example, U.S. Pat.No. 6,117,485 describes a foaming tissue sealant for treating woundedtissue in a subject. The sealant can be formulated to include a compoundor composition of the invention. The sealant is useful for significantlydiminishing or preventing blood or fluid loss from injured tissues,organs or blood vessels, while also providing a barrier to infection.

It is further envisioned that the synergistic antibiotic compositions ofthe invention can be used to inhibit bacterial cell growth and biofilmformation in or on products or devices used for personal hygiene. Soap,toothpaste, dental floss, laundry detergent or moisturizing lotion areexamples of consumer products that would benefit from the inclusion of acompound or synergistic antibiotic composition of the invention. Inaddition, such a compound or composition can be included in a personalhygiene device such as a toothbrush, tongue depressor, or any other suchdevice which comes in contact with a tissue.

The following description sets forth the general procedures involved inpracticing this aspect of the present invention. To the extent thatspecific materials are mentioned, it is merely for purposes ofillustration and is not intended to limit the invention. Unlessotherwise specified, general cloning procedures, such as those set forthin Sambrook et al., Molecular Cloning, Cold Spring Harbor Laboratory(1989) (hereinafter “Sambrook et al.”) or Ausubel et al. (eds) CurrentProtocols in Molecular Biology, John Wiley & Sons (1998) (hereinafter“Ausubel et al.”) are used.

EXAMPLES Example 1

Quorum Sensing in Escherichia coli and Salmonella typhimurium

Assay conditions. V. harveyi reporter strain BB170 (with quorum-sensingphenotype Sensor 1⁻, Sensor 2⁺) can induce lux expression only throughSignaling System 2. Addition of 10% cell-free spent culture fluidprepared from V. harveyi strain BB152 (which contains the autoinducer-2analog) stimulates a roughly 1000-fold increase in luminescence, anincrease that is normalized to 100% activity in FIG. 1.

E. coli strain AB1157 and S. typhimurium strain LT2 were each grown for8 h in LB broth or LB broth containing 0.5% glucose and the E. coli orS. typhimurium cells removed from the growth medium. Addition of 10%cell-free culture fluid maximally induced luminescence in the reporterstrain BB170, similar to culture fluids from V. harveyi BB152 (FIG. 1A).Specifically, E. coli AB1157 produced 106% and S. typhimurium produced237% of the V. harveyi BB152 activity.

In control: experiments, E. coli and S. typhimurium grown in LB withoutadded glucose did not produce the signaling factor, nor did blanksolutions containing 10% (v/v) of LB medium containing 0.5% glucose.Glucose, amino acids, cAMP, acetate, homoserine lactone, -ketoglutarateand other keto acids that are known to be excreted lacked activity.

Analogous experiments were performed with the V. harveyi reporter strainBB886 (Sensor 1⁺, Sensor 2⁻). V. harveyi BB886 is defective in itsresponse to signaling molecules that act through the Signaling System 2detector, but it is an otherwise wild type strain (Bassler et al., Mol.Microbiol. 13: 273-286, 1994). FIG. 1B shows the normalized 100%activation of V. harveyi BB886 by cell-free spent culture fluidsprepared from V. harveyi BB120. V. harveyi BB120 produces the System 1autoinducer N-(3-hydroxybutanoyl)-L-homoserine lactone (Bassler et al.,1993, supra). Addition of S. typhimurium LT2 and E. coli AB1157cell-free culture fluids to V. harveyi strain BB886 caused a 5% and a 1%increase above the control level (FIG. 1B). Together the results ofFIGS. 1A and 1B show that the signaling molecule produced by E. coli andS. typhimurium acts specifically through V. harveyi Signaling System 2and not some other, unidentified pathway.

FIG. 2 shows that viable E. coli AB1157 and S. typhimurium LT2 areRequired for Secretion of the Signaling Molecule.

Growth of E. coli AB1157 and S. typhimurium LT2 in LB medium containingglucose do not simply remove some pre-existing inhibitor of induction ofluminescence. Washed E. coli and S. typhimurium cells added directly tothe luminescence assay.

E. coli AB1157 and S. typhimurium LT2 were grown for 8 h in LBcontaining 0.5% glucose, the cells removed by centrifugation, and thecell pellets washed and resuspended in sterile V. harveyi luminescenceassay medium. E. coli AB1157 or S. typhimurium LT2 cells (1×10⁶ cells)were added to the diluted V. harveyi BB170 culture at the start of theexperiment.

The presence of washed E. coli AB1157 or S. typhimurium LT2 cells fullyinduces Lux expression in V. harveyi BB170 (FIG. 2, left-hand bar ineach series)(821-fold and 766-fold, respectively). Identical aliquots ofthe washed E. coli or S. typhimurium cells killed with short waveultraviolet light before addition to the assay did not stimulateluminescence (FIG. 2, right-hand bar for each strain). Taken together,the results show that E. coli AB1157 and S. typhimurium LT2 cellsproduce the stimulatory factor themselves during the experiment.

E. coli DH5α Does Not Produce the Signaling Activity. Clinical isolatesof E. coli and Salmonella also produce the signaling compound. Tenclinical isolates of Salmonella and five pathogenic isolates of E. coliO157 were assayed and all produced the activity. It was conceivable thatthe signal was some normal byproduct of glucose metabolism that simplydiffuses out of the cells. This is not the case however, because we showthat E. coli DH5α, which is equally capable of utilizing glucose as E.coli AB1157 and S. typhimurium LT2, does not produce the signalingactivity. FIG. 1A demonstrates that unlike E. coli AB1157 and S.typhimurium LT2, the addition of 10% cell-free culture fluid preparedfrom E. coli DH5α grown 8 h in LB containing 0.5% glucose does notstimulate light production in V. harveyi BB170. Similarly, inclusion ofwashed viable or killed E. coli DH5α cells in the luminescence assaydoes not stimulate V. harveyi BB170 to produce light (FIG. 2). Theinability of E. coli DH5α to produce the activity indicates that thishighly domesticated strain lacks the gene or genes necessary for eitherthe production or the export of the signaling activity. We assayed otherlaboratory strains of E. coli for the signaling activity (Table 1). OnlyE. coli DH5α was completely defective in producing the extracellularsignal.

The induction of luminescence in V. harveyi reporter strain BB170 bycell-free culture fluids from V. harveyi, S. typhimurium and E. coli isshown. Cell-free culture fluids were prepared from various strains of V.harveyi, S. typhimurium and E. coli as described and tested forproduction of a signaling substance that could stimulate lightproduction in the reporter strain V. harveyi BB170. The level of V.harveyi stimulation was normalized to 100%. The data for the 5 h timepoint are shown.

TABLE 2 Induction of Species and Strain Luminescence (%) V. harveyiBB152 100 S. typhimurium LT2 237 E. coli AB1157 106 E. coli DH5α  5 E.coli JM109  76 E. coli MG1655 100 E. coli MC4100  93

Glucose Regulates the Production and Degradation of the Signaling Factorby S. typhimurium LT2. Cell-free culture fluids from S. typhimurium LT2and E. coli AB1157 cells grown in LB without added glucose did notstimulate the expression of luminescence in the reporter strain,indicating that metabolism of glucose is necessary for the production ofthe signal. We tested other carbohydrates, and in general, growth in thepresence of PTS sugars (see Postma et al., in Escherichia coli andSalmonella Cellular and Molecular Biology, (F. C. Niehardt (ed), Am.Soc. Microbiol., Washington D.C., pp. 1149-1174, 1996) enabled E. coliAB1157 and S. typhimurium LT2 to produce the signal. Of the sugarstested, growth on glucose induced the synthesis of the highest level ofactivity. Growth on other carbon sources, for example TCA cycleintermediates and glycerol did not induce significant production of thesignaling activity.

We tested whether the presence of glucose was required for the cells tocontinue to produce the signal. FIG. 3 shows results with S. typhimuriumLT2 grown in LB containing limiting (0.1%) and non-limiting (0.5%)glucose concentrations. FIG. 3A shows that when glucose is limiting, S.typhimurium LT2 produces the signal in mid-exponential phase: (after 4 hgrowth), but stops producing the signaling activity once glucose isdepleted from the medium. FIG. 3B shows that when glucose does notbecome limiting, S. typhimurium LT2 produces greater total activity andcontinues to produce the signaling activity throughout exponentialphase, with maximal activity at 6 h growth. Furthermore, the Figure alsoshows that the signaling activity synthesized by mid-exponential phasecells is degraded by the time the cells reach stationary phase. Inconditions of limiting glucose, no activity remained at stationaryphase, and when glucose was plentiful, only 24% of the activityremained. Increasing the concentration of glucose in the. growth mediumdid not change these results, i.e., the activity was secreted duringmid-exponential growth, and severely reduced activity remained in thespent culture fluids by stationary phase.

In sum, the results presented in this example show that E. coli and S.typhimurium produce a signaling substance that stimulates one specificquorum-sensing system in V. harveyi. Many other bacteria have previouslybeen assayed for such an activity, and only rarely were speciesidentified that are positive for production of this factor (Bassler etal., 1997, supra). Furthermore, as shown here, the E. coli and S.typhimurium signal is potent; these bacteria make activity equal to thatof V. harveyi. The degradation of the E. coli and S. typhimurium signalprior to stationary phase indicates that quorum sensing in thesebacteria is tuned to low cell densities, suggesting that quorum sensingin E. coli and S. typhimurium is regulated so that the response to thesignal does not persist into stationary phase. Additionally, quorumsensing in E. coli and S. typhimurium is influenced by severalenvironmental factors. The production and the degradation of the signalare sensitive not only to growth phase but also to the metabolicactivity of the cells. These results indicate that the quorum-sensingsignal in E. coli and S. typhimurium has two functions; it allows thecells to communicate to one another their growth phase and also themetabolic potential of the environment.

Understanding the regulation of quorum sensing in E. coli and S.typhimurium is important for understanding community structure andcell-cell interactions in pathogenesis. In the wild, pathogenic E. coliand S. typhimurium may never reach stationary phase because dispersionis critical. It is therefore appropriate that quorum sensing in E. coliand S. typhimurium should be functioning at low cell density. Thissituation is in contrast to that of V. fischeri, the luminescent marinesymbiont, where the quorum-sensing system is only operational at highcell densities; cell densities indicative of existence inside thespecialized light organ of the host. The specific quorum-sensing systemsof V. fischeri and E. coli and S. typhimurium appear appropriatelyregulated for the niche in which each organism exists. In both cases,quorum sensing could be useful for communicating that the bacteriareside in the host, not free-living in the environment. Additionalcomplexity exists in the E. coli and S. typhimurium systems becausethese bacteria channel both cell density information and metabolic cuesinto the quorum-sensing circuit. Again, signals relaying informationregarding the abundance of glucose or other metabolites couldcommunicate to the bacteria that they should undergo the transition froma free-living mode to the mode of existence inside the host.

Under all the conditions we have tested, the signaling activitydescribed in this example does not extract quantitatively into organicsolvents and it does not bind to either a cation or anion exchangecolumn. Preliminary characterization indicates that the signal is asmall (less than 1000 MW) polar but apparently uncharged organiccompound. The activity is acid stabile and base labile, it is heatresistant to 80 but not 100° C. Purification of the E. coli, S.typhimurium and V. harveyi signal is described in greater detail in thefollowing examples.

Example 2

Regulation of Autoinducer Production in Salmonella typhimurium

In this example, the conditions under which S. typhimurium LT2 producesAI-2, the extracellular factor that stimulates lux expression in the V.harveyi Sensor 1⁻, Sensor 2⁺ reporter strain, are elucidated. Productionof the signaling molecule by S. typhimurium occurs during growth onpreferred carbohydrates that, upon utilization by the bacteria, resultin a decrease in the pH of the medium. Lowering the pH of the growthmedium in the absence of a preferred carbon source induces limitedproduction of the factor, indicating that the cells are influenced byboth the changing pH and the utilization of the carbon source. Thesignaling activity is degraded by the time the cells reach stationaryphase, and protein synthesis is required for degradation of theactivity. Osmotic shock following growth on an appropriate carbon sourcegreatly increases the amount of activity present in the S. typhimuriumculture fluids. This increased activity is apparently due to inductionof synthesis of the autoinducer and repression of degradation of theactivity. E. coli and S. typhimurium possess a protein called SdiA whichis homologous to LuxR from V. fischeri (Wang et al., EMBO J. 10:3363-3372, 1991; Ahmer et al., J. Bacteriol. 180: 1185-1193, 1998). SdiAis proposed to respond to an extracellular factor (Sitnikov et al.,Proc. Natl. Acad. Sci. USA 93: 336-341, 1996; Garcia-Lara et al., J.Bacteriol. 178: 2742-2748, 1996), and it has been shown to controlvirulence factor production in S. typhimurium (Ahmer et al., 1998,supra). The analysis set forth below shows that the AI-2 autoinducersignaling activity does not function through the SdiA pathway.

S. typhimurium LT2 Produces an Autoinducer-like Activity. Example 1demonstrates that S. typhimurium and E. coli strains produce a signalingactivity that stimulates lux expression in V. harveyi, and the signalingmolecule acts exclusively through the V. harveyi quorum-sensing System2. FIG. 4 shows the induction of luminescence in the V. harveyi System 2reporter strain BB170 (Sensor 1⁻, Sensor 2⁺). The control experimentshows the characteristic quorum-sensing behavior of V. harveyi (closedcircles). Immediately after dilution into fresh medium, the lightemitted per cell by V. harveyi drops rapidly, over 1000-fold. At acritical cell density, which corresponds to the accumulation of acritical concentration of endogenously produced autoinducer (AI-2) inthe medium, the luminescence per cell increases exponentially,approximately three orders of magnitude, to reattain the pre-dilutionlevel.

Addition of 10% cell-free culture fluid prepared from V. harveyi BB152(AI-1⁻, AI-2⁺) caused the reporter strain to maintain a high level oflight output following dilution (open circles). The increased lightoutput is due to the V. harveyi BB170 cells responding to the presenceof AI-2 in the cell-free culture fluids prepared from V. harveyi strainBB152 (Bassler etal., 1993, supra). Similarly, addition of cell-freeculture fluid from S. typhimurium LT2 grown in LB+0.5% glucose inducedluminescence in the reporter strain approximately 800-fold over thecontrol level (solid squares). No activity similar to V. harveyi AI-1was produced by S. typhimurium LT2 under these conditions and there isno AI-1 or AI-2 activity in LB+0.5% glucose (see Example 1).

Environmental Factors Influence Autoinducer Production and Degradationin S. typhimurium. Control of autoinducer production in S. typhimuriumis different than in other described quorum-sensing systems. FIG. 5Ademonstrates three important aspects of the regulation of autoinducerproduction in S. typhimurium. First, no autoinducer activity is observedwhen S. typhimurium is grown for 6 h in LB in the absence of glucose.Second, growth in the presence of glucose for 6 h results in substantialproduction of autoinducer (760-fold activation of the reporter strain).Third, activity, while detectable, is severely reduced when the S.typhimurium culture is allowed to grow to stationary phase (33-foldactivation of the reporter strain).

We subjected S. typhimurium LT2 to several different treatmentsincluding some environmental stresses in order to begin to understandwhat conditions favor autoinducer production versus those that favorautoinducer degradation. In the experiment presented in FIG. 5B, the S.typhimurium cells were induced for signal production by pre-growth in LBcontaining 0.5% glucose for 6 h. We have shown that under theseconditions, the glucose is not depleted (Surette and Bassler, 1998).After the induction phase of growth, the culture fluid was removed andaliquots of the cells were resuspended and incubated for 2 h under avariety of conditions that are described in the description of FIG. 2.Following each of these treatments cell-free fluids were prepared andtested for activity on BB170.

It is important to note that in the results presented in FIG. 5B, the S.typhimurium were pre-induced for autoinducer production at the start ofthe experiment, i.e., their cell-free culture fluid activated thereporter strain 760-fold. FIG. 5B shows that removal of the pre-growthculture fluid from these cells and resuspension of the cells in LBwithout glucose, in 0.1 M NaCl (hypotonic conditions), or heat shock at43° C. for 2 h resulted in no or very low autoinducer production. Theseresults indicate that the above treatments result in termination ofautoinducer production, or degradation of newly released autoinducer, orboth.

In contrast to the above results, resuspension of pre-induced cells infresh LB+glucose resulted in continued high-level production ofautoinducer (735-fold activation of the reporter). Similarly, acidic pHpromoted continued production of autoinducer (600-fold activation), andhypertonic osmotic shock (0.4 M NaCl) resulted in 1300-fold induction ofthe reporter. Increased AI-2 activity was only observed in the pH 5.0fluids or 0.4 M NaCl osmotic shock fluids of cells that were alreadyactively producing AI-2, i.e., if glucose was not included during thepre-growth, no measurable activity was produced following the identical2 h treatments.

Shifting S. typhimurium cells from LB+glucose to 0.4 M NaCl resulted inan accumulation of AI-2 activity to a level much greater than thatobserved under any other condition tested. Below it is shown that S.typhimurium cells resuspended in 0.4 M NaCl increase the biosynthesisand/or release of autoinducer, and furthermore they apparently do notdegrade significant quantities of the released activity. A similarincrease in AI-2 production occurs when the S. typhimurium cells areresuspended in 0.4 M NaCl, 0.4 M KCl or 0.8M sucrose, indicating thatthe NaCl effect on AI-2 production is an osmotic one, not an ionic one.This apparent osmotic shock effect on the S. typhimurium cells wasextremely useful because it enabled us to measure maximal release ofautoinducer activity in the absence of loss due to degradation.

The Effect of Glucose on Signal Production in S. typhimurium. In Example1 we showed that the continued presence of glucose was required for S.typhimurium to produce the quorum-sensing signaling factor. Becausesugar utilization both increases the growth rate while decreasing the pHof the culture, we further analyzed the effect of metabolism of glucose,decreasing pH and increasing cell number on signal production by S.typhimurium. In the experiment presented in FIG. 6, we measured signalproduction, growth rate, and pH in growing S. typhimurium LT2 culturescontaining limiting (0.1%) and non-limiting (1.0%) concentrations ofglucose. In the data presented in FIG. 6, at various times, the level ofautoinducer produced in both the cell-free culture fluids and in thecorresponding 0.4 M NaCl osmotic shock fluids was measured andnormalized for 1×10⁹ cells. It should be noted that unlike in FIG. 5,the cells in this experiment were not pre-induced for signal production.

FIG. 6 shows that the pattern of production and disappearance ofautoinducer observed in 0.4 M NaCl osmotic shock fluids mimics thatobserved in cell-free culture fluids. However, at every time point thatautoinducer is produced, much greater activity is detected in theosmotic shock fluids than in the corresponding cell-free culture fluids.Under conditions of limiting (0.1%) glucose (FIGS. 6A, 6C and 6E), S.typhimurium produces the signaling activity between 2-4 h (Bars).However, the glucose becomes completely depleted at 4 h, and at thattime production of the factor ceases (FIG. 6A). In contrast, when thecells are grown in 1.0% glucose (FIGS. 6B, 6D, and 6F), glucose ispresent in the medium throughout the entire experiment (FIG. 6B). Underthese conditions, the cells continue to synthesize activity for 12hours. Similar to the results shown in FIG. 5 and those reported inExample 1, almost no activity was observed in cell-free culture fluidsor osmotic shock fluids from stationary phase cells at 24 h regardlessof the glucose concentration.

S. typhimurium grows at roughly the same rate in both high and lowglucose media during exponential phase. In fact, the S. typhimuriumculture grown in high glucose medium does not reach the cell densityachieved by the S. typhimurium grown in the low glucose medium (FIGS. 6Cand 6D). Cell growth is probably inhibited in this culture by thedramatically reduced pH that occurs from increased glucose utilization.These results show that the higher level of activity produced by S.typhimurium in the LB containing 1% glucose is not due to higher cellnumber, but due to induction of signal production caused by glucosemetabolism.

FIGS. 6E and 6F show the pH of the low and high glucose cultures at eachtime point. Under conditions of low glucose (FIG. 6E), the pH of theculture initially decreases as the cells utilize the glucose. However,simultaneous to the complete depletion of the glucose, the pH begins torise. In contrast, under conditions of high glucose, the pH of themedium decreases to below pH 5 (FIG. 6F). In the experiments presentedin FIG. 6, both glucose catabolism and decreasing pH occursimultaneously suggesting that either or both of these factors could beresponsible for signal production by S. typhimurium.

Both Glucose Metabolism and Low pH Independently Control SignalProduction in S. typhimurium. To distinguish between the contributionfrom glucose metabolism and that from low pH in signal production by S.typhimurium, we compared the activity produced by S. typhimurium grownin LB containing 0.5% glucose in a culture in which the pH wasmaintained at 7.2 (FIG. 7A), to that produced by S. typhimurium grown inLB without glucose where the pH was maintained at 5.0 (FIG. 7B). Again,we measured the signal present in cell-free culture fluids and in 0.4 MNaCl osmotic shock fluids. Similar to the data presented in FIG. 3, thelevel of signal observed in cell-free culture fluids was lower than thatobserved in the 0.4 M osmotic shock fluids.

When S. typhimurium was grown in LB+0.5% glucose at pH 7.2 increasingamounts of the quorum-sensing signal were detected for 6 h. At 6 h, in0.4 M NaCl osmotic shock fluids, there was an approximately 550-foldstimulation of light production of the V. harveyi reporter strain BB170.No activity was produced after the 6 h time point. FIG. 7A shows thatthe pH was maintained between 7.15 and 7.25 for 8 h, after this time,the pH of the culture no longer decreased, but began increasingpresumably because the cells had depleted the glucose. We allowed the pHto continue to increase for the duration of the experiment. Also shownin the figure is the cell number at each time point. At pH 7.2, thecells grew rapidly and reached a high cell density.

Analysis of time courses similar to those presented here, has shown thatS. typhimurium does not produce any signal when it is grown in LBwithout glucose at neutral pH (see Example 1). However, S. typhimuriumdid transiently produce the quorum-sensing factor in the absence ofglucose when grown at pH 5.0 (FIG. 7B). Signal was produced for 4 h, andabout 450-fold stimulation of the reporter was the maximum activityachieved in 0.4 M NaCl osmotic shock fluids. Very little signal wasproduced by 5 h, and signal was completely absent after 6 h ofincubation. FIG. 7B shows that the pH was maintained between 5.0 and 5.2in this experiment. Note that the cells grew much more slowly at pH 5.0than at pH 7.2.

Preliminary Characterization of the S. typhimurium AutoinducerDegradative Apparatus. The quorum-sensing activity produced by S.typhimurium LT2 is degraded by the onset of stationary phase. We havedetermined that the activity contained in cell-free culture supernatantsand 0.4 M NaCl osmotic shock fluids from cells grown for 6 h inLB+glucose is stable for at least 24 h at 30° C., indicating that nodegradative activity is present in these cell-free fluids. Furthermore,mixing cell-free culture fluids prepared from actively producing S.typhimurium (i.e., from cultures grown for 6 h in LB+glucose) withcell-free culture fluids prepared from S. typhimurium that have degradedthe factor (i.e., from cultures grown for 12 or 24 h in LB+glucose) doesnot result in degradation of the activity. This result indicates thatthe degradative activity is not released, but instead, is associatedwith the cells.

We show in FIG. 5 that no further autoinducer is produced if S.typhimurium cells that are actively releasing autoinducer are shifted to0.1M NaCl. However, when these same cells are shifted to 0.4 M NaCl, weobserve even greater autoinducer production. This result implies thatlow osmolarity could be a signal that induces the autoinducerdegradative machinery. To begin to analyze the mechanism by whichosmolarity affects autoinducer production and degradation in S.typhimurium, we investigated the requirement for protein synthesis insignal production and degradation by S. typhimurium in high and lowosmolarity. As described in the legend to FIG. 5, S. typhimurium LT2 wasgrown in LB containing 0.5% glucose to achieve maximal induction ofsignal production then treated with 0.1M or 0.4 M NaCl in the presenceand absence of protein synthesis. Cell-free fluids were prepared andtested for signaling activity. Because half of the cell-free osmoticshock fluids contained chloramphenicol (Cm), V. harveyi JAF305 was usedas the reporter strain in the activity assay. This V. harveyi straincontains a Cm^(r) cassette in the luxN gene, and its phenotype is Sensor1⁻, Sensor 2⁺, a phenotype identical to that of V. harveyi BB170.

When the cells were resuspended in 0.4 M NaCl, the S. typhimuriumproduced and released increasing amounts of the signal for 200 min (FIG.8A, open squares). After this time, the level of signaling activitypresent in the cell-free osmotic shock fluid decreased somewhat,suggesting that some of the released signal was degraded. Quitedifferent results were obtained when the S. typhimurium cells wereresuspended in 0.1M NaCl (FIG. 8B, open squares). In this case, at earlytime points, the S. typhimurium produced a quantity of activityequivalent to that produced by cells resuspended in 0.4 M NaCl. However,by 120 min, no activity remained in the cell-free low osmolarity fluid.This result indicates that under conditions of low osmolarity, thereleased activity is rapidly degraded. We do not observe degradation ofthe activity in cell-free culture fluids, indicating that thedisappearance of the activity from low osmolarity cell-free fluids isnot due to chemical instability of the signaling molecule.

Under conditions of high osmolarity, when the cells were treated with Cmto inhibit protein synthesis, only about one quarter of the activity wasproduced compared to untreated cells. The closed squares in FIG. 8A showthat 300-fold induction of the reporter strain occurred in the presenceof Cm as compared to 1200-fold induction with the untreated cells (FIG.8A, open squares). When the S. typhimurium was resuspended in lowosmolarity (FIG. 8B), roughly three-quarters of the activity produced inthe absence of Cm (open squares) was produced in the presence of Cm(closed squares). In the presence of Cm, the released activity was notdegraded by 300 min in high osmolarity and only partially degraded inlow osmolarity.

To show that high osmolarity does not inhibit AI-2 signal degradation,we added the activity contained in the 0.4 M NaCl cell-free osmoticshock fluids to S. typhimurium cells that had been resuspended in 0.1MNaCl for two hours. As shown in FIG. 8, these are cells that can degradethe factor. Table 3 shows that these S. typhimurium cells degradedgreater than 98% of the signaling activity while incubated at highosmolarity. The table also shows that S. typhimurium cells that had beenincubated in 0.4 M NaCl (these are cells that are actively producing thesignal) released no further activity when resuspended in the 0.1M NaClincubation fluid obtained from the actively degrading cells.Furthermore, mixing active and inactive 0.4 M and 0.1M cell-free osmoticfluids did not result in degradation of the activity in the 0.4 Mfluids.

TABLE 3 High osmolarity induces release and low osmolarity inducesdegradation of the S. typhimurium signaling factor Treatment Foldinduction of Luminescence 0.1 M NaCl activity^(a) 4 0.1 M NaClactivity^(a) 4 0.4 M NaCl activity^(a) 944  0.1 M cells + 0.4 Mactivity^(b) 17  0.4 M cells + 0.1 M activity^(c) 6 ^(a) S. typhimuriumwas grown for 6 h in LB containing 0.5% glucose. The cells were pelletedand resuspended in either 0.1 M or 0.4 M NaCl for 2 h. Cell-free fluidswere prepared and tested for activity. ^(b) S. typhimurium cells thathad been incubated in 0.1 M NaCl for two hours were pelleted andresuspended in the activity contained in the cleared osmotic shockfluids obtained from cells suspended in 0.4 M NaCl for 2 h. Cell-freefluids were prepared after a 2 h incubation and assayed for signalingactivity. ^(c) S. typhimurium cells that had been suspended in 0.4 MNaCl were pelleted and incubated for 2 h in the cleared osmotic shockfluids obtained from cells suspended for 2 h in 0.1 M NaCl. Cell-freefluids were prepared after the 2 h incubation and assayed for signalingactivity.

The LuxR Homolog SdiA is not Involved in Response to the AI-2Autoinducer. A gene homologous to luxR of V. fischeri has beenidentified in E. coli and S. typhimurium and is called sdiA. Two reportssuggest that in E. coli, SdiA modestly regulates the expression of thecell division locus ftsQAZ in response to a factor present in cell-freeculture fluids (Garcia-Lara et al., 1996, supra), and in response to afew homoserine lactone autoinducers (Sitnikov et al., 1996, supra).Completion of the sequence of the E. coli genome shows that no LuxIhomologue exists in E. coli so the locus responsible for thebiosynthesis of the hypothesized soluble factor(s) has not beendetermined. Overexpression of SdiA in S. typhimurium has recently beenshown to influence the expression of several ORFs located on the S.typhimurium virulence plasmid (Ahmer et al., 1998, supra). As in the E.coli studies, SdiA activity in S. typhimurium is proposed to beregulated by an extracellular factor.

It was possible that the AI-2 autoinducer that we have beencharacterizing in S. typhimurium and E. coli acted through SdiA. Wetested whether AI-2 had an effect on genes regulated by SdiA in E. coliand S. typhimurium. In E. coli, we assayed an ftsQ1p2p-lacZ reporter,and in S. typhimurium we assayed an rck::MudJ fusion in both an sdiA⁺and sdiA⁻ background. We tested the effects of addition of LB, 0.4 MNaCl, 0.4 M NaCl osmotic shock fluids containing AI-2 activity from S.typhimurium LT2, E. coli O157, and 0.4 M NaCl osmotic shock fluid fromE. coli DH5α. We have shown previously in Example 1 that DH5α does notproduce AI-2 activity under our growth conditions.

For the E. coli experiments we determined that MC4100 and MC4100/pMS209(containing ftsQ1p2p in the incorrect orientation) had nomeasurable-galactosidase activity. The level of -galactosidase producedby MC4100/pMS207 (containing the ftsQ1p2p-lacZ fusion) was roughly 20-30Miller units, and this level of activity did not change under any:of theconditions tested here. This level of activity of the fusion wascomparable to that reported previously (Sitnikov et al., 1996, supra;Garcia-Lara et al., 1996, supra). In the S. typhimurium SdiA studies,similar to Ahmer et al. (1998, supra), we obtained ˜30 Miller units ofrck::MudJ activity in the sdiA+background and this level was reduced to10 units in the sdiA⁻ background. No change in -galactosidase productionoccurred following the addition of Al-2 from E. coli or S. typhimurium.These results indicate that, if an extracellular factor exists thatregulates the activity of SdiA, under the conditions we have tested, itis not AI-2.

Quorum Sensing in E. coli and S. typimurium. We have developed aheterologous bio-assay that enables detection of an extracellularsignaling factor produced by S. typhimurium. The factor mimics theaction of AI-2 of the quorum-sensing bacterium V. harveyi, and it actsspecifically through the V. harveyi Signaling System 2 detector LuxQ.Results using lacZ fusions to the ftsQ and rck promoters indicate that,under our assay conditions, the AI-2 quorum-sensing factor does notsignal to SdiA, at least with respect to regulation of these genes. TheAI-2 quorum-sensing system is therefore involved in a different S.typhimurium and E. coli signal transduction pathway than the one(s)investigated previously.

S. typhimurium LT2 produces an amount of activity roughly equivalent tothat produced by V. harvey, with approximately 800-fold stimulation ofthe V. harveyi reporter strain BB170 upon addition of 10% S. typhimuriumcell-free culture fluids. The timing of lux induction and the shape ofthe response curve of V. harveyi to the S. typhimurium signal areindistinguishable from those of V. harveyi responding to its own AI-2.Furthermore, we have been successful at partially purifying both the V.harveyi AI-2 and the S. typhimurium signal molecule using identicalpurification procedures. These two results lead us to believe that theS. typhimurium signaling molecule is identical to or very closelyrelated to AI-2 of V. harveyi.

Growth Conditions Regulate Signal Production and Degradation in S.typhimurium. In this example, we further characterize the regulation ofthe signaling activity in S. typhimurium LT2. Accumulation of signalingactivity in S. typhimurium culture supernatants is maximal duringmid-exponential phase when the cells are actively using glucose in richmedium. Under these growth conditions, use of glucose is accompanied bya rapid drop in pH of the culture. The results demonstrate that eitherglucose metabolism or low pH induces S. typhimurium LT2 to produce thequorum-sensing factor, indicating that both glucose and acidity generateindependent signals for autoinducer production. In the presence ofglucose, when the pH is not maintained, probably both the decreasing pHand the presence of an appropriate carbon source contribute to theregulation of quorum sensing in S. typhimurium. The results also showthat production of the autoinducer ceases before stationary phase in thepresence of glucose at neutral pH and in the absence of glucose at lowpH. Therefore, a combination of acidic conditions and the absence ofglucose is not required to cue S. typhimurium to terminate production ofautoinducer.

In addition to glucose, growth on several other carbohydrates alsoinduces production of the signaling activity. These include both PTS(fructose, mannose, glucitol, and glucosamine) and non-PTS (galactose.and arabinose) sugars. These findings eliminate an exclusive role forthe PTS in the regulation of autoinducer biosynthesis. When the S.typhimurium LT2 are grown on several other carbon sources (acetate,glycerol, citrate and serine) no significant accumulation of signalingactivity is observed. Example 1 shows that the signal is not any of anumber of substances known to be secreted by S. typhimurium, includingthe major products of mixed acid fermentation. Clearly, the cellsprecisely regulate production of the signaling molecule and favor itsproduction when growing on preferred carbohydrates. Identification ofthe signaling molecule and cloning of the biosynthetic gene(s) will aidin a fuller understanding of the regulation process.

This example shows that, in contrast to other quorum-sensing systems,the S. typhimurium signal does not accumulate in stationary phase.Autoinducer production and degradation both contribute to thisregulation. This example establishes autoinducer production as anincrease in the signaling activity present in cell-free fluids. Activitycould increase from release of newly biosynthesized autoinducer, releaseof stored autoinducer, repression of degradation of autoinducer, or somecombination of these. We define autoinducer degradation as thedisappearance of signaling activity from the cell-free fluids. Thisdisappearance could be due to destruction of the autoinducer, re-uptakeof the autoinducer, or a combination of these activities. Autoinducerproduction and degradation could occur simultaneously under someconditions. These findings indicate that quorum sensing in S.typhimurium is regulated such that the signal and presumably theresponse to the signal do not persist into stationary phase. Becausesignal production requires use of a preferred carbohydrate, quorumsensing in S. typhimurium may be used for measuring both the celldensity and the potential of the environment for growth.

Osmolarity Influences Signal Production and Degradation in S.typhimurium. S. typhimurium cells that are actively producing signal canbe further stimulated to produce signal by specific environmentaltreatments, such as 0.4 M NaCl osmotic shock, which indicates thatseveral independent regulatory pathways channel information intoautoinducer synthesis. On resuspension in 0.4 M NaCl, S. typhimuriumcells producing autoinducer exhibit significantly greater activity whenthey can synthesize protein than when protein synthesis is blocked.Furthermore, degradation of the signal also requires protein synthesis.

These results have several implications. First, in the presence of Cm,S. typhimurium resuspended at both high and low osmolarity produce asimilar amount of activity. This result indicates that, following growthin the presence of glucose, the S. typhimurium cells have a pre-definedcapacity to produce signaling activity (and/or to release alreadysynthesized activity from the cell). Second, resuspension of the cellsin high osmolarity medium increases signal production well beyond thislevel, which requires protein synthesis. High osmolarity is apparentlyone environmental cue that induces S. typhimurium to synthesize more ofthe biosynthetic apparatus necessary for signal production and/orrelease. Third, low osmolarity causes an initial release of activity,followed by a rapid degradation that requires protein synthesis becauseit does occur in the presence of Cm. These results imply that theenvironment has changed from conditions favoring autoinducer production(LB+a preferred carbohydrate, or high osmolarity) to conditions whereautoinducer production is not favored (low osmolarity, or absence of apreferred carbon source). This environmental change induces S.typhimurium to synthesize the protein(s) required for degradation of thesignaling activity.

When the S. typhimurium cells were incubated in 0.4 M NaCl nosignificant degradation of the activity occurred by 200 min. This resultindicates that either the necessary degradative protein(s) are notsynthesized under these conditions, or alternatively, the degradativeapparatus is assembled, but its activity is inhibited by highosmolarity. The results show that high osmolarity does not inhibitsignal degradation, because cells induced to degrade the activity can doso at high osmolarity. Therefore, the persistence of the activity in thehigh NaCl samples occurs because the degradation machinery is notsynthesized, not because its activity is inhibited.

It is difficult to determine precisely when S. typhimurium cells produceautoinducer and when they degrade it because both processes could occursimultaneously. It appears, however, that little or no degradationoccurs in high osmolarity, that conversion of cells from overall signalproducers to overall signal degraders occurs in low osmolarity and thatdegradation requires protein synthesis. Preliminary characterizationindicates that degradation is cell-associated, because the autoinduceractivity is stable in cell-free culture supernatants for long periods.In addition, combining active with inactive cell-free culture fluids oractive and inactive high and low osmolarity cell-free fluids does notpromote degradation of the auto inducer.

The Role for Quorum Sensing in Salmonella Pathogenesis. The observationspresented here on the regulation of signal production and degradation byS. typhimurium LT2 implicate a role for quorum sensing in pathogenesisof Salmonella. The conditions favoring signal production (nutrient rich,high osmolarity and low pH) are those likely to be encountered upon thefirst interaction of an enteric pathogen with its host. Conditionsfavoring degradation of the signal (nutrient poor, low osmolarity) arethose most probably encountered as the pathogen exits the host. Theinitial colonization of the host may be a concerted effort between apopulation of cells coordinated through this cell-cell signaling system.Other cues, that we have not yet tested, could also regulate quorumsensing in S. typhimurium. These may represent independent oroverlapping signaling pathways involved in pathogenesis. We areisolating S. typhimurium mutants to test these hypotheses. Finally,Salmonella pathogenesis is a dynamic process of interaction between thehost and metabolically active bacteria. Consistent with a role forquorum sensing in pathogenesis, our evidence suggests that thisquorum-sensing system is not functioning during stationary phase. Wehave shown that the signaling molecule is not produced during stationaryphase, and furthermore, existing signal is degraded. Perhaps quorumsensing is critical for S. typhimurium to undergo the transition betweena host-associated and a free-living existence.

Example 3

Quorum Sensing in Escherichia coli, Salmonella typhimurium and Vibrioharveyi: A New Family of Genes Responsible for Autoinducer Production

Genes responsible for AI-2 production in V. harveyi, E. coli and S.typhimurium (named luxS_(V.h.), luxS_(E.c.), and luxS_(S.t.)respectively) are highly homologous to each other, and are thought todefine a new family of proteins involved in autoinducer production. Thegenes have been identified in many bacteria by genome sequencingprojects, but until now no function has been ascribed to them in anyorganism. The luxS genes do not bear homology to any other gene known tobe involved in autoinducer production.

Identification and Cloning of the Gene Responsible for AI-2 Productionin V. harveyi

Previous examples show that, unlike many other E. coli strains, E. colistrain DH5α does not produce an AI-2 signal molecule that can bedetected by V. harveyi. We reasoned therefore, that we could use E. coliDH5α as a mutant to clone the V. harveyi AI-2 production gene. A libraryof wild type V. harveyi BB120 genomic DNA was transformed into E. colistrain DH5α, and the transformants were screened for AI-2 production inthe V. harveyi BB170 AI-2 detection bioassay. The library consisted of2,500 clones each containing roughly 25 kb of V. harveyi genomic DNA.Five DH5α clones were identified that resulted in upwards of 300-foldstimulation of the reporter strain in the bioassay.

The recombinant cosmid DNA from the five AI-2 producing E. coli DH5αclones was analyzed by restriction analysis and Southern blotting. Allfive of the cosmids contained an overlapping subset of identical V.harveyi genomic restriction fragments, indicating that we had cloned thesame locus several times. One cosmid, called pBB2929 was selected forfurther analysis. Random mutagenesis using transposon Tn5 was carriedout on cosmid pBB2929, and pools of cosmids harboring Tn5 insertionswere subsequently transformed into E. coli DH5α. We tested 962individual E. coli DH5α/pBB2929::Tn5 strains for the loss of the abilityto produce AI-2. Four E. coli DH5α strains harboring Tn5 insertions inpBB2929 were identified that failed to produce AI-2. We mapped thelocations of these Tn5 insertions in pBB2929 and found that all fourtransposon insertions resided in the same 2.6 kb HindIII V. harveyigenomic DNA fragment (FIG. 9A).

Cosmid pBB2929 was digested with HindIII and the 8 resulting fragmentswere subcloned in both orientations into pALTER (Promega). The pALTERsubclones were transformed into E. coli DH5α, and subsequently testedfor AI-2 production. The only strains capable of producing AI-2contained the 2.6 kb HindIII fragment identified in the Tn5 mutagenesis.This fragment was sequenced, and only one open reading frame (ORF) couldbe identified, and its location corresponded to the map positions of thefour Tn5 insertions that eliminated AI-2 production. We named the ORFLuxS_(V.h.) (FIG. 9A).

Mutagenesis of luxS_(V.h.) in V. harveyi. We analyzed the effects ofluxS_(V.h.) null mutations on AI-2 production in V. harveyi. The fourTn5 insertions that mapped to the LuxS_(V.h.) gene and the control Tn5insertion adjacent to the luxS_(V.h.) locus were transferred to thecorresponding locations in the V. harveyi BB120 chromosome to makestrains MM37, MM30, MM36, MM38 and MM28, respectively (FIG. 9A).Southern blotting was used to confirm the correct placement of all fiveTn5 insertions in the V. harveyi chromosome. The four V. harveyiluxS_(V.h.)::Tn5 insertion strains were tested for the ability toproduce AI-2, and all four strains gave identical results.

In FIG. 10A, we show the AI-2 production phenotypes of the wild typecontrol Tn5 insertion strain MM28 and one representativeluxS_(V.h.)::Tn5 insertion strain, MM30. V. harveyi MM28 and MM30 weregrown to high cell density, after which cell-free culture fluids wereprepared. The culture fluids were assayed for AI-2 activity by theability to induce luminescence in the AI-2 detector strain BB170. FIG.10A shows that addition of culture fluids from the control Tn5 insertionstrain MM28 induced luminescence in the reporter 780-fold, while culturefluid from the luxS_(V.h.)::Tn5 insertion strain MM30 did not induce theexpression of luminescence in the reporter. Therefore, a null mutationin luxS_(V.h.) in V. harveyi eliminates AI-2 production.

Identification and Analysis of S. typhimurium Autoinducer ProductionMutants. To identify the gene responsible for AI-2 production in S.typhimurium, we randomly mutagenized S. typhimurium LT2 using the MudJtransposon (Maloy et al., 1996, supra). Ten-thousand S. typhimurium LT2insertion mutants were assayed for AI-2 production in the V. harveyiBB170 bioassay. One S. typhimurium MudJ insertion mutant (strain CS132)was identified that lacked detectable AI-2 in culture fluids atmid-exponential phase.

FIG. 10B shows the AI-2 production phenotypes of S. typhimurium strainLT2 and the corresponding MudJ insertion strain CS132. The strains weregrown to mid-exponential phase in LB containing glucose, and cell-freeculture fluids were prepared and assayed for AI-2. S. typhimurium LT2culture fluids induced the reporter strain 500-fold, while culturefluids from strain CS132 contained no AI-2 activity. Furthermore, strainCS132 did not produce AI-2 under any of the growth conditions that wehave previously reported induce AI-2 production in S. typhimurium (notshown).

The site of the MudJ insertion in S. typhimurium CS132 was determined byPCR amplification followed by sequencing of the 110 bp of chromosomalDNA adjacent to the transposon. This sequence was used to search thedatabase for DNA homologies. The sequence matched a site (89/105 bpidentity) in the E. coli MG1655 genome that corresponded to an openreading frame of unknown function denoted ygaG (Blattner et al., 1997,supra). In the chromosome, the E. coli ygaG gene is flanked by the gshAand emrb genes (FIG. 9B). The ygaG gene is transcribed from its ownpromoter which is located immediately upstream of the gene, indicatingthat it is not in an operon with gshA. The emrB gene is transcribed inthe opposite direction. We PCR amplified the ygaG region from thechromosomes of E. coli O157:H7 and E. coli MG1655, and the two E. coliygaG genes were cloned into pUC19.

Complementation of S. typhimurium and E. coli AI-2⁻ Mutants. We testedwhether the E. coli O157:H7 ygaG gene and the V. harveyi luxS_(V.h.)gene could restore AI-2 production in the AI-2⁻ strains S. typhimuriumCS132 and E. coli DH5α. In FIG. 11A, we show the AI-2 activity producedby wild type V. harveyi BB120, E. coli O157:H7 and S. typhimurium LT2.In this figure, the level of AI-2 activity present in V. harveyi BB120cell-free culture fluids was normalized to 100%, and the activities incell-free culture fluids from E. coli and S. typhimurium compared tothat. In this experiment, E. coli O157:H7 produced 1.5 times and S.typhimurium LT2 produced 1.4 times more AI-2 activity than V. harveyiBB120 (i.e., 150% and 141%, respectively).

FIGS. 11B and 11C show the AI-2 complementation results for S.typhimurium CS132 and E. coli DH5α. FIG. 11B demonstrates thatintroduction of the E. coli O157:H7 ygaG gene into S. typhimurium CS132restored AT-2 production beyond the level of production of wild type S.typhimurium (i.e., 209% activity). Comparison of the data in FIGS. 11Aand 11B shows that the E. coli ygaG gene in S. typhimurium resulted inAI-2 production exceeding that produced in vivo by E. coli O157:H7.Introduction of the V. harveyi LuxS_(V.h.) gene into S. typhimuriumresulted in AI-2 production at slightly less than the level produced bywild type V. harveyi BB120 (i.e., 73% of the level of V. harveyi BB120).FIG. 11C shows that E. coli DH5α was also complemented to AI-2production by both the cloned E. coli O157:H7 and the V. harveyi BB120AI-2 production genes. However, introduction of E. coli O157:H7 ygaG andV. harveyi BB120 luxS_(V.h.) into E. coli DH5α resulted in only 31% and43% of the V. harveyi BB120 AI-2 activity, respectively. FIGS. 11B and11C show that the control vectors produced no activity in thecomplementation experiments.

Analysis of the AI-2 Production Genes from V. harveyi, E. coli and S.typhimurium. We sequenced the AI-2 production gene LuxS_(V.h.) from V.harveyi BB120 and the ygaG loci from E. coli O157:H7, E. coli MG1655 andE. coli DH5α. The translated protein sequences encoded by the ygaG ORF'sare shown in FIG. 12, and they are aligned with the translated LuxSprotein sequence from V. harveyi. The non-bold, underlined amino acidsindicate the residues in the E. coli proteins that differ from the V.harveyi LuxS protein. The ygaG loci from E. coli encode proteins thatare highly homologous to one another and also to LuxS from V. harveyi.The E. coli MG1655 (SEQ ID NO: 25) and the E. coli O157:H7 (SEQ ID NO:11) YgaG proteins are 77% and 76% identical to LuxS from V. harveyiBB120 (SEQ ID NO: 10). The DNA sequence we determined for ygaG from E.coli O157:H7 differs at five sites from the reported (and our) sequencefor the E. coli MG 1655 ygaG gene. Four of the changes are silent, thefifth results in a conservative Ala to Val alteration at amino acidresidue 103 in the E. coli O157:H7 protein.

Identification of the ygaG locus in E. coli MG1655 and E. coli O157:H7allowed us to investigate the AI-2 production defect in E. coli DH5α. E.coli DH5α possesses the ygaG gene because we could PCR amplify thisregion from the chromosome using the same primers we employed to amplifyit from E. coli MG1655 and E. coli O157:H7. Examination of the E. coliDH5α ygaG promoter showed that it is identical to that of E. coliMG1655, indicating that the AI-2 defect in E. coli DH5α is not simplydue to decreased transcription of ygaG. However, sequence analysis ofthe E. coli DH5α ygaG coding region showed that a one G-C base pairdeletion and a T to A transversion exist at bp 222 and 224,respectively. The frameshift mutation resulting from the G/C deletioncauses premature truncation of the E. coli DH5α protein. FIG. 12 showsthat the truncated E. coli DH5α protein is 111 amino acids, while the E.coli MG1655 and E. coli O157:H7 proteins are 171 residues. Twentyaltered amino acids are translated after the frame shift and prior totermination of the protein. Our complementation results (FIG. 11)demonstrate that the AI-2 production defect in E. coli DH5α is recessiveto in trans expression of ygaG, which is consistent with the defectbeing due to a null mutation caused. by the frame shift in the E. coliDH5α ygaG gene.

We searched the S. typhimurium database using the sequence we obtainedadjacent to the MudJ that inactivated the AI-2 production function in S.typhimurium CS132. A perfect match (110/110 bp) was identified tofragment B_TR7095.85-T7 in the S. typhimurium LT2 genome-sequencingdatabase (Genome Sequencing Center, Washington University, St. Louis).However, the S. typhimurium LT2 database ygaG sequence (SEQ ID NO: 26)is incomplete (FIG. 12). The translated sequence matches the E. coli andV. harveyi sequences beginning at amino acid residue 8. The translatedsequence shows that the S. typhimurium protein is 75% identical to LuxSof V. harveyi. In order to align the S. typhimurium sequence with the V.harveyi LuxS protein, we corrected three apparent frame shift errors inthe database sequence. Considering that only crude, unannotated sequencedata is currently available for S. typhimurium, we predict that the S.typhimurium protein contains seven more amino acids, and that the frameshift mutations are sequencing errors. We were unsuccessful at PCRamplifying either the S. typhimurium 14028 or the S. typhimurium LT2ygaG gene using the primers designed for E. coli, so we do not yet havethe complete sequence of the S. typhimurium gene.

The results set forth above indicate that the genes we have identifiedand analyzed encode a novel family of proteins responsible forautoinducer production. Members of this new family of genes, referred toherein as LuxS, are highly homologous to one another but not to anyother identified genes. The encoded product of the LuxS genes catalyzean essential step in the synthesis of the signaling molecules of thepresent invention.

Example 4

Construction of a Sensor 1⁻, AI⁻2⁻ V. harveyi Reporter Strain

V. harveyi null mutants in each of the lux genes luxL, luxM, luxN, luxSand luxQ fail either to make or to respond to one specific autoinducer,but they still produce light because, in each case, one quorum-sensingsystem remains operational. A double luxN, luxS V. harveyi mutant doesnot emit light without the addition of exogenous AI-2 because thismutant does not respond to AI-1 and it does not produce AI-2.

The V. harveyi LuxS gene has been cloned into E. coli DH5α on a broadhost range mobilizable cosmid called pLAFR2. This construction restoresAI-2 production to E. coli DH5α. A marked null mutation was engineeredinto the luxS gene by introducing a chloramphenicol resistance (Cm^(r))cassette into an internal restriction site. Placement of the Cm^(r)cassette at this site in luxS subsequently eliminated AI-2 production inE. coli DH5α.

The luxS::Cm^(r) null allele was transferred onto the chromosome of V.harveyi strain BB170. Strain BB170 contains a Tn5Kan^(r) in luxN anddoes not respond to AI-1. To construct the double mutant, triparentalconjugations were carried out by mixing stationary phase cultures of E.coli DH5α carrying the V. harveyi luxS::CM^(r) construction in pLAFR2(pLAFR2 carries tetracycline resistance), E. coli DH5α carrying the tradonor plasmid pRK2013 and the V. harveyi recipient strain BB170.Exchange of the luxS::Cm^(r) mutant allele for the wild type luxS alleleon the chromosome occurs by homologous recombination. The exogenotecosmid in V. harveyi was eliminated by the introduction of a secondincompatible plasmid pPH1JI. This was accomplished by mating E. coliDH5α containing pPH1JI with the V. harveyi BB170 recipient containingthe luxS::Cm^(r) cosmid, and selecting for exconjugants on platescontaining ampicillin (for counter selection of the E. coli donor)chloramphenicol (for inheritance of the mutant luxS::Cm^(r) allele) andgentamicin (for maintenance of the plasmid pPH1JI). Southern blotanalysis was used to verify that the exogenote pLAFR2 cosmid has beeneliminated and that the luxS::Cm^(r) construction had been transferredto the corresponding position in the genome of V. harveyi. The pPH1JIcosmid was subsequently eliminated by growth in the absence ofgentamicin selection.

Verification that the LuxN, LuxS Double Mutant Responds to AI-2. The Vharveyi strain that is mutant in luxN and luxS was stimulated to producelight in response to the exogenous addition of AI-2 but not AI-1. Thiswas verified in a luminescence assay for response to V. harveyi AI-1 andAI-2. V. harveyi strain MM30 (luxS::Tn5) which is phenotypically AI-1⁺,AI-2⁻, and V. harveyi strain BB152 (luxM::Tn5) which is phenotypicallyAI-1⁻, AI-2⁺ were used as the sources of AI-1 and AI-2, respectively.The AI-1 and AI-2 present in culture fluids of these strains was testedfor stimulation of light production of the V. harveyi LuxN, LuxS doublemutant reporter strain. In this assay, autoinducer preparations fromMM30, BB152 or sterile medium controls were added to the wells ofmicrotiter plates, followed by the addition of the V. harveyi reporterstrain. The resulting light production was monitored using a liquidscintillation counter in the chemiluminescence mode. Maximal stimulationof light production in the V. harveyi luxN, luxS reporter strain wascompared to that produced by the Sensor 1⁺, Sensor 2⁻ V. harveyi strainBB886 and the Sensor 1⁻, Sensor 2⁺ V. harveyi strain BB170. These two V.harveyi strains are routinely used in this assay as reporters of AI-1and AI-2 activity, respectively.

Determine Optimum Concentrations of AI-2 in Microtiter Assays. Theaforementioned screen will be optimized for use in 96-well microtiterassays. The screen will be used in inhibitor assays for identifyinginhibitors of AI-2. Purified or synthetic AI-2 will be added to themicrotiter wells containing the newly constructed reporter strain andinhibition will be measured by a decrease in light emission from thewells containing an inhibitor. The assay will be optimized bydetermining the concentration of cells and AI-2 in the microtiter wellsthat will allow for maximal sensitivity. The optimal AI-2 concentrationwill be that which stimulates half-maximal light output for a givenconcentration of cells per unit time. Initial experiments will beconducted in this concentration range to determine the range of AI-2concentration that produces the greatest change in light output. Similarexperiments using AI-1 and a non self-stimulating sensor-1⁺, sensor-2⁻mutant (BB886) showed that the assay was sensitive to concentrations aslow as 100 nM AI-1 and that light emission was linear over 6 orders ofmagnitude (light emission from a self-stimulating strain was linear over3 orders). Similar results for AI-2 using the new reporter strain thatwill not self-stimulate and therefore have zero background lightemission are predicted. Light emission from the microtiter wells will bemeasured with a Wallac TriLux liquid scintillation counter model1450-021 in the chemiluminescence mode. This machine will accommodate 16plates and will therefore allow for 1536 separate concentrationexperiments per run.

Example 5

In-Vitro Method for Synthesizing AI-2; Purification and Identificationof AI-2

Several lines of evidence show that autoinducer-2 is not aacyl-homoserine lactone. Autoinducer-2 resists purification byconventional techniques used for the isolation of acyl-homoserinelactone autoinducers such as AI-1 from V. harveyi. Unlike otheracyl-homoserine lactone autoinducers, AI-2 activity does not extractquantitatively into organic solvents. Furthermore, autoinducer-2 failsto bind to either a cation or anion exchange column. The presentcharacterization of autoinducer-2 indicates that it has a molecularweight of less than 1000 kDa, and is a polar but apparently unchargedorganic compound. The AI-2 activity is acid-stable, base-labile, andwithstands heating to about 80° C. but not 100° C. The luxS genesidentified bear no homology to other genes known to be involved inproduction of HSL autoinducers further indicating that the present AI-2class of autoinducers is novel.

Thus, in addition to providing a cloned, overexpressed, and purified S.typhimurium LuxS protein, the present invention also provides a methodfor producing AI-2 in vitro. The present invention provides a mechanismfor generating large quantities of pure AI-2 useful for mass spectraland NMR analysis, and for screening compounds that regulate the activityof AI-2. Moreover, the present invention provides a method fordetermining the in vivo biosynthetic pathway for AI-2 synthesis.

Analysis of the genomic locations of the various luxS genes identifiedin the present invention indicates that the luxS genes do notconsistently reside in any one location in the chromosome, nor do theytypically appear in close proximity to any specific gene(s). In onecase, however, the luxS gene is the third gene in a three-gene operonwith two genes (metk and pfs). In E. coli, Salmonella and many otherbacteria, MetK and Pfs are involved in the conversion of S-adenosylmethionine (SAM) to homocysteine and autoinducer-2 (FIG. 15). MetKconverts methionine to SAM, which is an important cofactor in one-carbonmetabolism. SAM methylates DNA, RNA, and a variety of cell proteins, andseveral SAM dependent methyl transferases act at this step. S-adenosylhomocysteine (SAH) results from transfer of the methyl group from SAM toits substrates. SAH strongly inhibits SAM dependent methyltransferases.Therefore, bacteria rapidly degrade SAH via the enzyme Pfs. Thedesignation “pfs” refers to an open reading frame in the E. coli genomethat has recently been determined to encode the enzyme5′-methylthioadenosine/S-adenosylhomocysteine nucleosidase, also knownas MTA/SAH nucleosidase. In the present system, the enzyme cleaves theglycosidic bond in S-adenosylhomocycteine (SAH). Thus, Pfs converts SAHto adenine and S-ribosyl homocysteine. In a final step, S-ribosylhomocysteine undergoes cleavage to homocysteine and autoinducer-2.Homocysteine can re-enter this pathway after methylation to generatemethionine, which MetK can convert to SAM.

Catabolism of SAH is a salvage pathway for recycling metabolicintermediates (adenine and homocysteine). Some bacteria, however,eliminate SAH by removing adenosine directly from SAH to generatehomocysteine. Cells that use this second mechanism do not produceautoinducer-2. In the pathway shown in FIG. 15, the enzyme responsiblefor conversion of S-ribosyl homocysteine to4,5-dihydroxy-2-cyclopenten-1-one or 4-hydroxy-5-methyl-2h-furan-3-onewas not previously identified, cloned, or purified.

LuxS is involved in the pathway shown in FIG. 15, and SAM and SAH areinvolved in AI-2 production. The structure of AI-2 can be4,5-dihydroxy-2-cyclopenten-1-one or 4-hydroxy-5-methyl-2h-furan-3-one,in which case LuxS is the uncharacterized enzyme that acts on S-ribosylhomocysteine. Second, LuxS could act on one of the intermediates to makeAI-2. LuxS would represent a branch point off the known pathway.

To confirm that LuxS is involved in the conversion of SAM to AI-2, thegene encoding the S. typhimurium LuxS protein was cloned, overexpressedand the S. typhimurium LuxS protein was purified. This protein was usedin combination with dialyzed cell-free extracts prepared from a S.typhimurium luxS null mutant to show that addition of SAM and LuxSprotein could restore AI-2 production to dialyzed LuxS− cell extracts.Reaction mixtures were prepared containing 10 mM Sodium Phosphate bufferpH 7.0, dialyzed S. typhimurium LuxS− cell extract and SAM. PurifiedLuxS protein was added to some of these mixtures. The reactions wereincubated at room temperature for 60 min, followed by centrifugation ina 5000 MWCO centricon. The material with MW<5000 was added to thestandard V. harveyi bioassay as previously described. Dialyzed LuxS−cell extracts to which SAM was added or extracts containing LuxS proteinwithout the addition of SAM produced no AI-2 activity. However,identical extracts to which LuxS protein and SAM had been added producedAI-2 that resulted in over 500-fold stimulation in light production inthe bioassay.

Further investigation showed that SAM is not the direct substrate forLuxS, and that LuxS must act at a step subsequent to the conversion ofSAM to SAH (FIG. 15). It was determined that AI-2 was not produced ifSAM was added directly to LuxS protein, however activity was produced bypre-incubation of SAM with the LuxS− extracts, filtration, andsubsequent addition of LuxS protein to the filtrate. Importantly, thesestudies indicate that SAM can react with an element in the cell extractbefore it can be used by LuxS to make AI-2. Presumably, the SAMdependent methyl transferases present in the cell extract use SAM as amethyl donor and convert it to SAH in the process. To verify this, SAHwas substituted for SAM in an in vitro assay. Addition of SAH to the invitro assay resulted in much greater AI-2 production than when SAM wasadded. This result indicates that LuxS functions in the pathwaysubsequent to the conversion of SAM to SAH. Again, addition of SAHdirectly to LuxS protein is not sufficient for production of AI-2activity, while pre-incubation of SAH with dialyzed LuxS− extractsfollowed by filtration and subsequent addition of LuxS protein to thefiltrates does result in AI-2 production. Presumably SAH is converted toS-ribosyl homocysteine and then LuxS acts to produce AI-2.

The proposed pathway shown in FIG. 15 is not a salvage pathway forrecycling secondary metabolites, but rather is the pathway forproduction of AI-2. According to the invention, AI-2 is a derivative ofribose. It is noteworthy that, in V. harveyi, LuxP, the primary sensorfor AI-2, is a homologue of the E. coli and S. typhimurium ribosebinding protein.

Example 6

Bioassay for Inhibitor of the AI-1 Mediated Quorum Sensing Pathway

The quantitative assay for detection of an autoinducer-1 quorum sensingsystem derives from a previous report by in M. Manefield et al,Microbiol 145, 283-291(1999).

In one example of this bioassay, test compounds such as the halogenatedfuranones of Structure VII are dissolved in ethanol for use in thecurrent assay.

Synthetic OHHL (N-3-(oxohexanoyl)-L-homoserine), the AI-1 autoinducer inV. fischeri, prepared according to the method of A. Eberhard et al. ArchMicrobiol 146, 35-40 (1986), is dissolved in ethyl acetate for use inthe assay. [3H]OHHL is prepared based on the method of H. Kaplan et al.,J Label Compd Radiopharm 22, 387-395 (1985).

Bioluminescence is quantified as relative light units on a liquidscintillation counter. After addition of OHHL (10 nM to 100 nM OHHL) andthe test compounds (up to 100 μM) to dilute 10 mL cultures(OD600<0.0005) the luminescence response of 100 μL samples is measuredin triplicate. Appropriate concentrations of ethanol solvent areincorporated into control treatments. Growth is monitored by followingthe OD600 of 10 ml cultures in appropriate media from lag-, throughexponential- into stationary-phase growth.

Example 7

Bioassay for Inhibitors of the Peptide-Mediated Quorum Sensing Mechanism

The assay for detection of a peptide-mediated quorum sensing system isbased on a previous report described in M. Otto et al., FEBS Lett. 450,257-262. (1999). S. epidermidis Tü3298 (DSM) is the wild-type teststrain and the host for the promoter test plasmid. S. aureus strainstested for δ-toxin production are S. aureus Newman, 8325-4, SA113, ATCC12600, RN4220, and ATCC 33591 of Otto et al. (1999). S. aureus RN6390 isa prototypic strain from which the following mutant strains are derived:S. aureus RN6911 “agr−” an isogenic mutant carrying an agr::getMmutation, “sar−” carrying a sar::Tn917LTV1 mutation, and “agr−/sar−”carrying both a sar::Tn917LTV1 and an agr::tetM mutation of A. L. Cheunget al., J. Clin. Invest. 94, 1815-1822 (1994). The promoter test plasmidinserted into S. epidermidis Tü3298 contains the promoterless pUB112 catgene of R. Brückner et al., EMBO J. 4 2950-2300 (1985) adjacent to amultiple cloning site and carries an erythromycin-resistance gene ermBfrom transposon Tn551. Plasmid pRB594P3 is constructed by insertion of aBamHI-digested PCR product of the agr P3 region of S. epidermidis ATCC14990 into the BamHI site of the multiple cloning site.

S. epidermidis cells grown in TSB or BM (‘basic medium’: 1% tryptone(Difco), 0.5% yeast extract (Gibco BRL), 0.5% NaCl, 0.1% K2HPO4, 0.1%glucose) are disrupted in 20 mM Tris-HCI (pH 7.8) by glass beads asdescribed in C. Sizemore et al., Mol. Gen Genet. 227, 377-384 (1991).Cell debris is removed by centrifugation (10 min, 5000×g). Membranefractions are prepared by additional ultracentrifugation of the crudecell extract at 10500×g for 1 h. Surface-associated proteins areisolated by boiling cells at 100° C. for 5 min and centrifugation (10min, 5000×g). Surface proteins are isolated by incubating cells withlysostaphin for 10 min at 37° C. and centrifugation (10 min, 5000×g).Chromosomal staphylococcal DNA is prepared according to the method of J.Mamur, J. Mol. Biol. 3, 208-218 (1961). Proteins are separated bytricine-SDS-PAGE according to H. Schägger, H. Anal. Biochem. 166,368-379 (1987) using Bio-Rad Protean IIxi chambers and a separationlength of 16 cm.

Crude peptides are isolated on a Waters 600 Multi Solvent DeliverySystem equipped with a Lambda Max Model 481 as detector. Asemi-preparative column (Nucleosil C18, 4×250 mm; 5 m; Grom, Herrenberg,Germany) is eluted at a flow rate of 3.5 ml/min with a linear gradient(10-100% B in A in 45 min; solvent A: 0.1% trifluoroacetic acid (TFA) inwater; solvent B: 0.1% TFA in acetonitrile). The detection wavelength is214 nm. The concentration of purified peptides, redissolved indimethylsulfoxide (DMSO), is determined using analytical HPLC on aKontron HPLC System with Kroma System 2000 software. An analyticalcolumn (Spherisorb ODS2 2×100 mm; 5 μM; Grom, Herrenberg, Germany) iseluted at a flow rate of 250 μl/min with a linear gradient (0-100% B inA in 30 min; solvent A: 0.1% TFA in water; solvent B: 0.1% TFA inacetonitrile). The detection wavelength is 214 nm. A known amount of the(unmodified) peptide DSVCASYF is used as a reference. The amount ofdelta-toxin is quantified using the same system. A Pharmacia ResourcePHE 1 ml column is eluted with 1.5 column volumes of a linear gradient(0-100% of B in A; A: 0.1% TFA in water; B: 0.1% TFA in acetonitrile).The S. epidermidis delta-toxin is eluted using the same conditions on aAKTA explorer 100 system (Amersham Pharmacia Biotech, Freiburg,Germany). The isolated delta-toxin is chemically analyzed by ESI-MS.

CAT activity is determined according to the method of W. V. Shaw, (1975)Methods Enzymol. 43, 737-755. The assay mixture contained 100 mMTris-HCL (pH 7.8), 0.1 mM acetyl-coenzyme A and 0.4 mg5,5′-dithiobis-2-nitrobenzoic acid (DTNB/ml). Assays are performed in 96well microtiter plates using a SpectraMax 340 microtiter plate reader(Molecular Devices, Sunnyvale, Calif. USA) with SpectraMaxPro software.Cell extract (5 μl) and 5 mM chloramphenicol in 100% ethanol (5 μl) (or5 μl 100% ethanol in controls) are added to 90 μl of the assay mixture.Cell extracts are diluted 1:10 or 1:100 with 20 mM Tris-HCL (pH 7.8)when necessary. Absorption at 412 nm is measured every 15 s for 20 min.The linear part of the resulting curve is used to determine the CATactivity (absorption coefficient ε=13600 1/M for DTNB). For calculationof the specific activity, protein contents of the cell extracts aredetermined using the Bio-Rad DC protein assay for detergent-containingsamples (Bio-Rad Laboratories GmbH, Munich, Germany).

SDS-polyacrylamide gels are blotted onto nitrocellulose membranes(Schleicher and Schuell BA 83) using the semi-dry blotting technique.Blots are blocked overnight with 5% skim milk. The first antibody isapplied for 2 h at a concentration of 1:20,000 (anti-α-toxin) or1:40,000 (anti-protein A). After washing, the blots are incubated withanti-IgG-coupled HRP from Amersham Pharmacia (1:5000) for 1 h. Alldilutions are made in Tris-buffered saline (TBS: 10 mM Tris-HCl, pH 7.4,150 mM NaCl). Signals are detected with the ECL detection system(Amersham Pharmacia Biotech, Freiburg, Germany).

Blood plates are prepared with sheep blood agar base (Oxoid) to which 5%defibrinated sheep blood is added. Samples are spotted onto filters,which are dried and then laid on agar plates and incubated at 37° C. forat least 24 h.

Example 8

Antibiotic Susceptibility Assay

Antimicrobial susceptibility testing was conducted according to theNational Committee for Clinical Laboratory Standards (NCCLS) referencemethod “Broth Dilution Procedure (Microdilution)” published January 1977(UPDATE VERSION). The method yields a minimum inhibitory dose (MIC)required for complete inhibition of bacterial growth. MICs weredetermined using a dilution series of antibiotic, in which all of thewells contained a constant concentration of the inhibitor compound wasmaintained. In addition, before the instant susceptibility tests wereperformed, the inhibitor compounds were tested in the appropriateinhibitor screens (See, for example, FIG. 32 for the AI-2 inhibitor2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone). Once their inhibitoryactivity is demonstrated in screens, the inhibitors were also tested forantibiotic activity. Experiments were conducted in 96 well microtiterplates using a final volume of 0.1 ml/well. Assays were conducted usingeither Mueller-Hinton broth, Todd-Hewitt broth, or Nutrient Broth(Difco). The bacterial innoculum was prepared from a log phase overnightculture of Streptococcus pyogenes ATCC 19615 or Staphylococcus aureusATCC 25923. Turbidity of the cultures was adjusted with saline to 0.05McFarland standard (10⁷CFU/ml), and 5 microliters of this innoculum wasadded to each well. The inhibitor compounds were prepared by dissolvinga stock solution in water. Working stocks of quorum inhibitors compoundswere made by diluting the stock solutions with bacterial broth. Sodiumsalts of the antibiotics were used in these experiments. A stocksolution (10 mg/ml) was prepared as stipulated by the manufacturer bydissolving a weighed amount of antibiotic in water or DMSO. Allantibiotics were added in two-fold serial dilutions to a series of wellsto yield final concentrations ranging from 100 μg/ml to 0.1 μg/ml. Thesingle exception was sulfisoxazole where the range of final doses rangedfrom 300 μg/ml to 2.5 μg/ml. Bacterial broth was used as the diluent.The range of antibiotic concentrations used were chosen to be at andbelow the MIC for the antibiotic alone. Cultures were sealed andincubated for 20 hours at 37° C. MIC values were determined byspectrophotometric measurements of absorbance at 600 nm. The MIC isdefined as the lowest concentration of antibiotic that completelyinhibits growth of 99% the test organism in the tubes. Fold-changes. inMIC concentration were determined by comparing the MIC for antibioticand quorum inhibitor compounds with the MIC measured using antibioticalone.

Using the above antimicrobial assay, the combination of the quoruminhibitor compound 2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone incombination with either vancomycin, ciprofloxacin or sulfisoxazoleshowed marked synergies against the test strain. The quorum inhibitorcompound did not inhibit cell growth (FIG. 33). Vancomycin alone had anMinimum Inhibitory Concentration (MIC) of approximately 100 μg/ml; whenit was combined with the inhibitor compound at a concentration of 5μg/ml it had approximately the same MIC, when it was combined with thequorum inhibitor compound at 12.5 μg/ml it had an MIC of approximately1.6 micrograms/milliliter. Vancomycin had the same MIC when theconcentration of the quorum inhibitor compound was increased to 50μg/ml. Finally, with the inhibitor alone, the MIC was greater than 100μg/ml. Against the same test strain, ciprofloxacin alone has a MIC of0.8 μg/ml. In combination with the same quorum inhibitor molecule at aconcentration of 25 μg/ml, ciprofloxacin displayed a MIC of 0.4 μg/ml.Again, when the inhibitor was tested alone the MIC was greater than 100μg/ml. Against the same test strain sulfisoxazole alone exhibited an MICof approximately 300 micrograms per milliliter, while in the presence ofa concentration of 100 micrograms per milliliter of the quorum inhibitorcompound it exhibited a MIC of approximately 100 μg/ml. As before, theinhibitor compound alone demonstrated and MIC of greater than 100micrograms per milliliter. Against the other test strain,Staphlylococcus aureus, ampicillin alone had a MIC of 1.6 μg/ml, whilein the presence of the inhibitor compound (25 μg/ml) the antibiotic hada MIC of 0.4 μg/ml.

Example 9

Isolation of Halogenated Furanones

Many of the halogenated furanones of Structure VII are extracted fromtheir host bacteria according to protocols established by R. de Nys,Tetrahedron 49, 11213-11220(1993). Algal tissue is frozen, freeze-dried,extracted with dichloromethane and reduced in vacuo. Pure compounds areisolated from this crude extract by vacuum liquid chromatography andHPLC, and identified by 1H and 13C NMR spectroscopy.

Example 10

Preparation of Inhibitors of the Peptide Quorum-Sensing Mechanism

Cyclic peptides of the formula

(cyclo)-YSTCDFIM;

(cyclo)-GVNACSSLF;

(cyclo)-GVNASSSLF; and

(cyclo)-GVNA(DAPA)SSLF,

in which the C-terminal carbonyl group forms a thiolactone with thesulfur atom of the cysteine residue (YSTCDFIM and GVNACSSLF); a lactonegroup with the oxygen atom of the first serine residue (GVNASSSLF); oran amide bond with amino group of the diaminoproprionic acid (DAPA)residue (GVNA(DAPA)SSLF; are synthesized through use of the Fmoc/tBustrategy on Tritylresin (PepChem: Clausen and Goldammer, Tübingen,Germany). The sequence of the peptide is DSVXASYF, with cysteine (C),serine (S) or 1,3-diaminopropionic acid (Dpr) in the X position. Thecorresponding protected amino acids for the synthesis of cyclic peptidesare Fmoc-Cys(Mmt)-OH, Fmoc-Ser(Trt)-OH (both cleavable with TFA:TIS indichloromethane) and Fmoc-Dpr(Dde)-OH (cleavable with hydrazine). Thecyclic peptides are synthesized and purified according to M Otto, et al.(1998) FEBS Lett. 424, 89-94. The purity of peptides (>90%) iscontrolled by RP-C18 chromatography and ESI-MS.

Example 11

Characterization and Biosynthesis of an AI-2 Analog

The invention further provides a method for an in vitro procedure forlarge-scale production of pure AI-2. As indicated in FIG. 15, SAH is aprecursor in the LuxS dependent biosynthesis of AI-2. Furthermore, LuxSdoes not act directly on SAH. Prior to the action of LuxS, some enzymein dialyzed cell extracts must first act on SAH to convert it toS-ribosyl homocysteine by Pfs. Therefore the substrate for LuxS isS-ribosyl homocysteine.

To confirm that LuxS acts on S-ribosyl homocysteine, the Pfs enzyme canbe purified and used to convert SAH to S-ribosyl homocysteine. Towardthis end, the pfs gene has been cloned from S. typhimurium 14028 placedinto the overexpression vector pLM-1. The Pfs enzyme will beoverexpressed and SAH will be added to purified Pfs to produce S-ribosylhomocysteine. The conversion of SAH to S-ribosyl homocysteine will beconfirmed by reverse phase HPLC analysis (SAH is UV active whileS-ribosyl homocysteine is not). Subsequently, the S-ribosyl homocysteineproduced by Pfs will be added to purified LuxS. Following incubation,the mixture will be filtered over a 5000 MWCO centricon. The filtratewill be tested for AI-2 activity in the previously described V. harveyibioassay.

Regulation of LuxP or LuxQ Activity

It is an object of the invention to provide compounds and methods forregulating the activity of autoinducer-2 receptors such as LuxP or LuxQ.Compounds of the invention include those that interact with LuxP orLuxQ. Specifically, the invention provides a method for the regulationof LuxP or LuxQ protein resulting in the regulation of bacterial cellgrowth or the regulation of bacterial pathogenicity by regulating theexpression of a factor associated with bacterial virulence. The methodof the invention envisions contacting LuxP or LuxQ with pentenomycin, orderivatives thereof, such that LuxP or LuxQ activity is regulated.Pentenomycin has previously been identified as having antibioticactivity. The present study provides the first data indicating thatpentenomycin acts as an inhibitor of AI-2 initiated activation of abiochemical pathway. The chemical structure of pentenomycin, andderivatives thereof (see below), is/are similar to that of the structureof autoinducer-2 as identified in the present study.

The present invention provides a basis for the rational design ofderivatives and analogs of AI-2 for regulating bacterial growth andpathogenicity. Such analogs and derivatives can be used to regulate theactivity of those proteins involved in the autoinducer-2 signalingpathway, such as LuxP or LuxQ.

An autoinducer-2 (AI-2) molecule of the invention can interact withLuxP, the protein encoded by the homologue of the luxP gene ofpathogenic bacteria such as V. cholerae, S. typhimurium and E. coli. Inturn, the AI-2-LuxP complex can interact with LuxQ, which is the proteinproduct encoded by the luxQ gene. The AI-2-LuxP-LuxQ interaction canpromote luminescence in bacteria such as Vibrio spp by activating theexpression of genes involved in luminesence. In addition, theAI-2-LuxP-LuxQ interaction has been linked to the activation ofbiochemical pathways required for bacterial pathogenicity. Thus, theinvention provides a method for controlling bacterial gene expressionand for regulating bacterial pathogenicity by regulating AI-2-LuxP-LuxQinteractions using an AI-2 analogue, such as pentenomycin. For example,an AI-2 analogue can compete with endogenous AI-2 for binding to LuxP orLuxQ proteins thereby providing a means for regulating the activity ofthe protein.

The present invention further provides examples of AI-2 analogs capableof inhibiting AI-2 activated luminescence in the V. harveyi luminescenceassay (see FIGS. 16-18). These AI-2 analogs have not previously beenshown to have antimicrobial activity or act as an inhibitor of AI-2initiated activation of a biochemical pathway. Examples of such analogsinclude:

FIG. 16 shows the results of screening assays of AI-2 analogues. FIG. 16panels A and B show the results of a 6 hour assay using compounds 6, 9,15 and 18 (panel A) and compounds 3, 4, 7 and 13 (panel B) on teststrain BB170. FIG. 16 panels C and D show the effect of the samecompounds on control strain JAF78. Strain BB170 synthesizes AI-2starting at 4.5 hours into the assay. Light produced at the start of theassays is from AI-2 carried over from cells diluted from stationaryphase. Strain JAF78 is a mutant strain in which light production is“locked on” and is unaffected by the presence or absence of autoinducer.Increase in light over the time course reflects increase in cellpopulation density. Compounds 6,9,15 and 18 produced approximately a100-fold decrease in light emission from the no-compound control at the6 hour time point in BB170 but no significant change in light emissionin JAF78 (panels A&C). Direct counts of cells plated from each treatmentshowed no significant differences in cell viability. Compounds 3,4,7 and13 produced no significant difference in light emission in either strain(panels B&D).

LuxO Regulation of Expression. At low cell density, in the absence ofautoinducer-2, the LuxQ sensor acts as a kinase. The sensorautophosphorylates conserved His residues and transfers the phosphorylgroup to conserved Asp residues in attached response regulator domains.Thus, the first phosphotransfer event is intra-molecular. Subsequently,inter-molecular phospho-transfer occurs from the LuxQ sensor to aconserved His residue of the phosphorelay protein LuxU. In the finalstep, the phosphoryl group is transferred to the conserved Asp in theresponse regulator protein LuxO. Phosphorylation of LuxO activates theprotein, and its function is to cause repression of the luxCDABEGHoperon. Therefore, at low cell density, the bacteria make no light. Athigh cell density, in the presence of autoinducer-2, LuxQ activity isaltered, switching from kinase to phosphatase activity. In this mode,the sensor drains phosphate out of the system. The phosphatase activityof the sensor results in rapid elimination of LuxO-phosphate, and thedephosphorylated form of LuxO is inactive. Therefore, at high celldensity, no repression of luxCDABEGH occurs, and the bacteria emitlight.

V. harveyi uses this complex quorum sensing system, specifically theLuxPQ/AI-2 quorum sensing circuit, to communicate between species.Therefore, V. harveyi monitors not only its own cell-population densitybut also that of other bacteria. This ability allows V. harveyi toregulate behavior based on whether it exists alone or in consortium.luxS, the gene encoding the AI-2 synthase, belongs to a highly conservedfamily of genes that specify AI-2 production in a wide range of bothGram-negative and Gram-positive bacteria, including E. coli, S.typhimurium, Salmonella typhi, Vibrio cholerae, Yersinia pestis,Staphylococcus aureus, Streptococcus pyogenes, Enterococcus faecalis,and Bacillus subtilis. Thus, various species of bacteria can use AI-2for inter-species communication. Moreover, the present study indicatesthat the presence of AI-2 initiates a cascade of events culminating inthe derepression (i.e., activation) of various genes. It is an object ofthe invention to provide compounds and methods for regulating AI-2activity such that the derepression/activation of downstream geneticelements is also regulated. To that end, the present study indicatesthat LuxO activates transcription of downstream target genes includingthe production of siderophore, as well as colony morphology (Table 4 andFIG. 20). These are the first examples of quorum sensing regulatedphenotypes, other than Lux, in V. harveyi clearly indicating that AI-2quorum sensing controls potentially pathogenic phenotypes.

In the present study, mutations in luxO (the gene encoding the LuxOprotein) and/or rpoN (the gene encoding the σ⁵⁴ protein) were tested todetermine if they affected siderophore production in V. harveyi. TheSchwyn and Neilands chromazurol S assay was used to measure siderophorereleased by different V. harveyi strains. The S assay quantitativelymeasures siderophore by optically assessing the color change thatchromazurol S undergoes when it loses its chelated ferric ion tosiderophore present in spent culture fluids. Regulation of siderophoreproduction in many species of bacteria including E. coli and V. choleraeis under the control of the ferric uptake regulation (Fur) protein. Inthese cases, under iron-rich conditions, the Fur protein binds Fe(II)ions and represses the transcription of genes required for siderophorebiosynthesis and transport. De-repression of these genes occurs duringperiods of iron deprivation, when Fur is not bound to Fe(II) The resultspresented in Table 4 indicate that LuxO and σ⁵⁴ have a role inactivating the production of siderophores.

TABLE 4 LuxO and σ⁵⁴ regulate siderophore production in V. harveyiSiderophore V. harveyi strain Genotype P_(lac)-rpoN^(a) units^(b) BB120wild type − 8 ± 3 JAF78 luxO::Cm^(r) − 7 ± 4 JAF548 luxO D47E − 50 ± 5 BNL240 rpoN::Cm^(r) − 3 ± 3 BNL240 rpoN::Cm^(r) + 6 ± 3 BNL244 luxOD47E, rpoN::Cm^(r) − 4 ± 1 BNL244 luxO D47E, rpoN::Cm^(r) + 25 ± 3 ^(a)The wild type V. harveyi rpoN gene was expressed under control ofthe lac promoter from plasmid pBNL2090 (Table 4). ^(b)Siderophoreproduction was measured using the chromazurol S assay (Schwyn andNeilands, 1987). Siderophore units were calculated according to themethod of Payne (1994), and normalized for cell number using theformula: 100 X [(OD₆₃₀ (media control) − OD₆₃₀ (spent culture fluid)) /OD₆₀₀ (cell culture)]. Values shown are the mean ± SEM of threeindependent experiments.

Wild type strain BB120, the −luxO strain JAF78, and the rpoN::Cm^(r)null strain BNL240 all produce similar amounts of siderophore (3 to 8units) when grown in AB minimal medium. In contrast, the presence ofactivated luxO D47E in JAF548 increases siderophore production to 50units. This result indicates that phospho-LuxO activates siderophoreproduction. Disruption of rpoN in the luxO D47E background (strainBNL244) reduces siderophore production to wild type levels (4 units),indicating that similar to what was shown above for Lux regulation,phospho-LuxO controls siderophore production when wild type σ⁵⁴ ispresent. In trans introduction of wild type rpoN into the luxO D47E,rpoN::Cm^(r) strain complements the defect. In this case, siderophoreproduction increased to 25 units, approaching that of the luxO D47Estrain. These results demonstrate that the activated form of LuxO, alongwith σ⁵⁴, has a role in regulation of siderophore production.

In addition to the siderophore production phenotype, the present studyshows that V. harveyi mutants possessing a constitutively activated LuxO(i.e., LuxO D47E or LuxN L166R) also consistently exhibit an alteredcolony morphology that is similar to the rugose colony morphologydescribed for V. cholerae and the opaque colony morphology described forVibrio parahaemolyticus. In V. cholerae, the rugose phenotype requires alarge gene cluster called vps that is necessary for the production ofthe exopolysaccharide rugose polysaccharide. In V. parahaemolyticus ahomologue of the V. harveyi LuxR transcriptional activator proteincalled OpaR is involved in the switch to the opaque phenotype. Vibriocholerae is the causal organism of the diarrheal disease cholera and therugose variants of V. cholerae have been shown to produce anexopolysaccharide matrix. The rugose polysaccharide has been shown toconfer increased resistance to a variety of agents such as chlorine,bioacids, and oxidative and osmotic stresses. In addition, the rugosephenotype promotes biofilm formation thereby increasing the survival ofthe organism in aquatic environments.

FIG. 20 is a photograph showing the colony morphologies of various V.harveyi strains. Colonies of wild type V. harveyi and the rpoN::Cm^(r)null strain are smooth and glassy in appearance, while colonies of theluxO D47E strain are wrinkled and opaque. The figure shows that thecolony morphology phenotype caused by the activated luxO D47E protein isdependent upon the presence of wild type rpoN because strain BNL244(luxO D47E, rpoN::Cm^(r)) has the wild type smooth colony morphology.Similar to that observed for rugose strains of V. cholerae, the V.harveyi luxO D47E mutant forms a pellicle when grown in liquid culture.Pellicle formation is also dependent on wild type rpoN. Identicalresults were obtained when the “locked” LuxN L166R strain JAF549 wasused in place of the LuxO D47E strain JAF548. The fact that a singleamino acid change in LuxO or LuxN can affect various phenotypesincluding siderophore production and colony morphology indicates thatLuxO and σ⁵⁴ are involved in the regulation of multiple target genes.

The inhibition of an AI-2 mediated response was further measured in theV. harveyi bioassay. Compound QXP031 was tested against V. harveyitester and control strains. As shown in FIG. 21, at the concentrationsindicated, compound QXP031 specifically inhibited AI-2 mediatedluciferase expression in V. harveyi as monitored by bioluminescenceintensity. The results are normalized to cell count and any minimaleffects seen in the control strain. The fold difference inbioluminescence intensity at the different drug concentrations versus nodrug control is indicated above the appropriate bars in FIG. 21.

In addition, the effect of a compound of the invention on the expressionof a virulence factor was measured in a CAMP assay. Many streptococciproduce a diffusible extracellular protein (CAMP) that actssynergistically with staphylococcal beta lysin to lyse erythrocytes ontrypticase soy agar plates containing sheep blood. Hemolysis oferythrocytes is an important component of the virulence response in manypathogenic bacteria. A single straight streak of a beta lysin producingS. aureus strain is made. Steptococci to be tested are streakedperpendicular to the S. aureus streak. After overnight incubation apositive test is characterized by an arrowhead-shaped zone of completehemolysis in the area into which both staphylococcal beta lysin andstreptococcal CAMP factor have diffused. Compound QXP031 was tested in aCAMP assay employing S. aureus and S. pyogenes pathogenic bacteria.Application of QXP031 resulted in a negative CAMP score as shown in FIG.22.

Proteinase activity is an important component of the virulence responsein many pathogenic bacteria. Skim milk containing agar plates can beused to score for proteinase activity in a variety of bacteria.Proteolytic activity is scored as a clearing zone surrounding a testinoculum. The clearing zone is the result of the proteolytic breakdownof the milk proteins suspended in the agar plates. Regions where milkprotein is not broken retain a milky opaque appearance. FIG. 23 showsthe inhibition of S. pyogenes proteolytic activity by QXP031.

Thus, the present invention to provide compounds and methods forregulating the effect of AI-2 on such targets. Provided herein arecompounds of structure I, II, III or IV and pharmaceutical compositionscomprising such compounds and methods of using the compounds andcompositions of the invention to regulate bacterial growth and virulenceby. regulating the activity of AI-2 and proteins that interact withAI-2. Thus, the invention provides a mechanism for the control ofbacterial growth, such as by inhibition of bacterial growth, utilizingthe compounds of the invention. The invention further provides amechanism to not only control bacterial growth but also to control thosepathways involved in expression of phenotypes associated with bacterialvirulence and pathogenicity such as siderophore production and rugosepolysaccharide production.

Example 12

Biofilm inhibition

Biofilm formation was measured using a microtiter-based assay.Free-swimming (planktonic) bacteria were cultured in AB or LB mediasupplemented with glucose in 96 well microtiter dishes. Biofilmstypically formed along the walls of the wells at the interface of theliquid and air phase. At the end of the incubation, aliquots of acrystal violet solution (stock 0.1%) were added to the wells to stainboth the adherent and the non-adherent cells. The wells were then washedwith deionized water to remove non-adherent cells, and the bound crystalviolet solubilized with 200 microliters of water. Absorbance reading at600 nm (A600) were used to quantitate the amount of crystal violet dyethat had adhered to the biofilms. When indicated, synthetic AI-2 wasadded to the wells at the beginning of the cultures.

Various genotypes of V. harveyi were tested for biofilm formation in theabsence of any exogenous AI-2 (FIG. 26). The MM32 strain (LuxN−, LuxS−)formed more biofilm that either the wild-type V. harveyi (strain BB120)or V. harveyi indicator strain BB170 which contains an inactivatingmutation in LuxN. The results were the same regardless of the whether ABmedia with glucose (Panel A) or LB media supplemented with glucose(Panel B) was used. These observations suggest that more biofilm isproduced by V. harveyi when the endogenous synthesis of AI-2 iseliminated.

As shown in FIG. 26, strains of V. harveyi were used to test the effectsof exogenous 4-hydroxy-5-methyl-2h-furan-3-one on biofilm formation.Various amounts of synthetic AI-2 were added to the initialfree-swimming bacterial cultures in LB media supplemented with glucose,and biofilm formation measured at the end of the incubation. The resultsindicate that AI-2 affects biofilm formation in all V. harveyi strains,and that the results are reproducible for each genotype. In the MM32strain, low doses of AI-2 block biofilm formation. In contrast, additionof the same low doses of AI-2 to wild-type V. harveyi (strain BB120) orV. harveyi indicator strain BB170 increases the extent of biofilm thatforms. Higher concentrations of AI-2 stimulated biofilm formation in allV. harveyi strains tested.

The effects of AI-2 on biofilm formation were also evaluated inPseudomonas aeruginosa (ATCC 27853) (FIG. 27). Biofilm formation by thisorganism is of particular interest because of the association ofPseudomonas aeruginosa biofilms with decreased lung capacity in subjectswith cystic fibrosis. Using AB media with glucose as the media, additionof exogenous synthetic AI-2 caused a dose-dependent increase in thelevel of biofilm formation by P. aeruginosa. The magnitude anddose-response to AI-2 was found to be pH-dependent in this system.

Materials and Methods

Strains and Media. The bacterial strains used and their genotypes andphenotypes are listed in Table 5.

TABLE 5 Bacterial Strains; Their Genotypes and Relevant PhenotypesStrain Genotype Relevant phenotype S. typhimurium LT2 Wild type E. coliO157 Wild type E. coli MG1655 F-, ilvG, rfb-50 Wild type E. coli MC4100(lac)U169, araD139, rpsL, thi LacZ- E. coli DH5α supE44, hsdR17, recA1,AI-2 endA1, gyrA96, thi-1, relA1 V. harvey BB170 luxN::Tn5 Sensor 1−,Sensor 2+ V. harveyi BB152 luxL::Tn5 AI-1−, AI-2+ V. harveyi JAF305luxN::Cm5 Sensor 1−, Sensor 2+

Luria broth (LB) contained 10 g Bacto Tryptone (Difco), 5 g YeastExtract (Difco) and 10 g NaCl per liter (Sambrook et al., 1989). Therecipe for Autoinducer Bioassay (AB) medium has been reported previously(Greenberg et al., Arch. Microbiol. 120: 87-91, 1979). LM medium(L-Marine) contains 20 g NaCl, 10 g Bacto Tryptone, 5 g Bacto YeastExtract and 15 g Agar per liter (Bassler et al., 1994, supra).Regulation of AI-2 production similar to that reported here was alsoobserved with the ATCC strain Salmonella enterica Serovar Typhimurium14028, an independent clinical isolate of Salmonella enterica SerovarTyphimurium, and nine other Salmonella enterica serovars (other thanTyphimurium).

Growth Conditions for S. typhimurium LT2 and Preparation of Cell-freeCulture Fluids. S. typhimurium LT2 was grown overnight in LB broth withshaking at 30° C. The next day, 30 μl of the overnight culture was usedto inoculate 3 ml of fresh LB broth. In cultures containing additionalcarbon sources, at the time of inoculation, 20% sterile stock solutionswere added to give the specified final concentrations. Followingsubculturing of the cells, the tubes were shaken at 200 rpm at 30 C. forthe time periods indicated in the text. Cell-free culture fluids wereprepared by removal of the cells from the culture medium bycentrifugation for 5 min at 15,000 rpm in a microcentrifuge. The clearedsupernatants were passed through 0.2 μm cellulose acetate Spin X filters(CoStar, Cambridge, Mass.) by centrifugation for 1 min at 8000×g.Samples were stored at −20 C. Similar results to those reported herewere obtained when we grew the S. typhimurium at 37° C. The preparationof cell-free culture fluids from V. harveyi strains has already beenreported (Bassler et al., 1993, supra; Bassler et al., 1997, supra).

Density-dependent Bioluminescence Assay. The V. harveyi reporter strainBBI70 (Sensor 1⁻, Sensor 2⁺) (Bassler et al., 1993, supra) was grown for12 h at 30° C. in AB medium, and diluted 1:5000 into fresh AB medium.Luminescence was measured as a function of cell density by quantitatinglight production at different times during growth with a Wallac Model1409 liquid scintillation counter (Wallac Inc., Gaithersburg, Md.). Thecell density was measured by diluting the same aliquots of cells usedfor measuring luminescence, spreading the dilutions onto solid LMmedium, incubating the plates overnight at 30° C., and counting theresulting colonies the following day. Relative Light Units are (countsmin⁻¹ ml⁻¹×10³)/(colony forming units ml⁻¹). Cell-free culturesupernatants from V. harveyi or S. typhimurium strains were added to afinal concentration of 10% (v/v) at the time of the first measurement.In control experiments, 10% (v/v) of AB medium, LB medium or LB mediumcontaining 0.5% glucose was added instead of cell-free culture fluids.

S. typhimurium Autoinducer Activity Assay. The quorum-sensing signalingactivity released by S. typhimurium LT2 was assayed following growthunder various conditions. 10 μl of cell-free culture fluids from S.typhimurium LT2 grown and harvested as described above were added to96-well microtiter dishes. The V. harveyi reporter strain BB170 wasgrown overnight and diluted as described above. Ninety microliters ofthe diluted V. harveyi cells were added to the wells containing the S.typhimurium cell-free culture fluids. Positive control wells contained10 μl of cell-free culture fluid from V. harveyi BB152 (AI-1⁻, AI-2⁺)(Bassler et al., 1993, supra). The microtiter dishes were shaken in arotary shaker at 200 rpm at 30° C. Light production was measured hourlyusing a Wallac Model 1450 Microbeta Plus liquid scintillation counterdesigned for microtiter dishes (Wallac Inc., Gaithersburg, Md.). Inthese experiments, the cell density was not measured at each time point.Rather, to ensure that increased light production was due to a signalingactivity and not a growth medium component, the luminescence productionby V. harveyi in wells containing cell-free culture fluids was comparedto that produced by V. harveyi in wells containing 10 μl of theidentical growth medium alone. Data are reported as fold-stimulationover that obtained for growth medium alone.

Factors Controlling Signal Production in S. typhimurium. S. typhimuriumLT2 was grown for 6 h in LB containing 0.5% glucose as described above.The mid-exponential phase culture was divided into several identicalaliquots. One aliquot of cells was grown to stationary phase (24 h at30° C. with shaking). In the remaining aliquots, the cells were removedfrom the LB-glucose growth medium by centrifugation for 5 min at 15,000rpm in a microcentrifuge. The resulting cell pellets were resuspended atan OD₆₀₀ of 2.0 in either LB, LB+0.5% glucose, LB at pH 5.0, or in 0.1MNaCl, or 0.4M NaCl (in water). The resuspended cells were shaken at 30°C. or 43° C. for 2 h. Cell-free fluids were prepared from the stationaryphase culture, and from the cells that had been resuspended andincubated in the various media or the osmotic shock solutions. Thecell-free fluids were tested for signaling activity in the S.typhimurium activity assay as described above.

Effects of Growth Phase, pH, Glucose Concentration and Osmolarity onAutoinducer Production by S. typhimurium. S. typhimurium LT2 was grownat 30° C. for various times in LB containing limiting (0.1%) andnon-limiting (1.0%) glucose concentrations. At the times specified inthe text, the cell number was determined by plating dilutions of the S.typhimurium cultures onto LB medium and counting colonies the followingday. The pH of the two cultures was measured, and the percent glucoseremaining in each culture was determined using the Trinder assay asdescribed in Example 1. Cell-free culture fluids were prepared from theLB-glucose cultures as described above. The same cells from which thecell-free culture fluids were prepared were resuspended in 0.4M NaClosmotic shock solution and shaken at 200 rpm, 30° C. for 2 h. Wedetermined that this timing was optimal for production of autoinducer.The cells were removed from the osmotic shock solution by centrifugationat 15,000 rpm for 5 min in a microcentrifuge. Cell-free osmotic shockfluids were prepared from the resuspended cells exactly as described forcell-free culture fluids. Signaling activity in both the cell-freeculture fluids and the cell-free osmotic shock fluids was assayed asdescribed above. In experiments in which the pH was maintained at 7.2,the cells were grown in LB+0.5% glucose containing 50 mM MOPS at pH 7.2.The pH was adjusted every 15-30 min using 1 M MOPS pH 7.2. Inexperiments performed at pH 5.0, LB broth was maintained between pH 5.0and 5.2 with 1M NaOH.

Requirement for Protein Synthesis in Signal Production, Release andDegradation by S. typhimurium LT2. S. typhimurium LT2 was pre-grown inLB containing 0.5% glucose at 30° C. to an OD₆₀₀ of 2.5 (approximately6-8 h). The culture was divided into four identical aliquots. Twoaliquots were treated with 100 μg/ml Cm for 5 min at room temperatureafter which the cells were harvested by centrifugation at 15,000 rpm for5 min. One Cm-treated cell pellet was resuspended in 0.1M NaClcontaining 30 μg/ml Cm, and the second pellet was resuspended in 0.4MNaCl containing 30 g/ml Cm. Each of these pellets was resuspended to afinal OD₆₀₀ of 2.0. The remaining two culture aliquots were not treatedwith Cm. Instead, the cells in these two aliquots were harvested bycentrifugation and resuspended in 0.1M and 0.4M NaCl exactly asdescribed for the Cm-treated cells. The cell suspensions were incubatedat 30° C. with shaking. At the times indicated in the text, 1.5 mlaliquots were removed from the cell suspensions and cell-free osmoticshock fluids were prepared by the procedure described above.

Analysis of the Effect of Autoinducer on SdiA Regulated Gene Expression.A sequence that includes the ftsQ1p and ftsQ2p promoters (Wang et al.,1991, supra) was amplified from E. coli MG1655 chromosomal DNA using thefollowing primers: ftsQ1p, 5′-CGGAGATCTGCGCTTTCAATGGATAAACTACG-3′;ftsQ2p, 5′-CGCGGATCCTCTTCTTCGCTGTTTCGCGTG-3′. The amplified productcontained both the ftsQ promoters and the first 14 codons of the ftsQgene flanked by BamHI and BglII sites. The ftsQ1p2p PCR product wascloned into the BamHI site of vector pMLB1034 (Silhavy et al.,Experiments with Gene Fusions, Cold Spring Harbor Press, 1984) togenerate a lacZ fusion that contained the promoters, ribosome-bindingsite, and initiation codon of ftsQ. A correctly oriented clone, pMS207,and a clone containing the ftsQ1p2p insert in the opposite orientation,pMS209, were chosen for further analysis. Both inserts were sequenced toensure that no errors were introduced during the PCR reaction.

For ftsQ regulation in E. coli, the plasmids pMS207 and pMS209 weretransformed into E. coli strain MC4100 (Silhavy et al., 1984, supra),and the transformants were grown overnight in LB containing 100 mg/Lampicillin at 30° C. with aeration. For rck regulation, S. typhimuriumstrains BA1105 (rck::MudJ) and BA1305 (rck::MudJ sdiA) were grownovernight in LB containing 100 mg/L kanamycin at 30° C. with aeration.The overnight cultures were diluted 20-fold into fresh medium and grownfor an additional 4.5 h. At this time, each culture was divided intofive identical aliquots and 10% (v/v) of one of the following was addedto each aliquot: LB, 0.4M NaCl, 0.4M osmotic shock fluids from S.typhimurium LT2, E. coli O157 or E. coli strain DH5α (negative control).The osmotic shock fluids were prepared as described above, followingpre-growth of the S. typhimurium LT2 and E. coli in LB containing 0.5%glucose for 6h. The cell suspensions were incubated at 30° C. for 2 h,after which standard-galactosidase reactions were performed on thesamples (Miller, A Short Course in Bacterial Genetics, Cold SpringHarbor Laboratory Press, 1992).

Preparation of Cell-free Culture Fuids. E. coli strains AB1157 and DH5αand S. typhimurium strain LT2 were grown at 30° C. overnight withaeration in LB broth containing glucose at the concentrations specifiedin the text. The following morning, fresh LB medium containing the sameconcentration of glucose used for the overnight growth was inoculated ata 1:100 dilution with the overnight grown cultures. The fresh cultureswere grown for various times at 30° C. with aeration. Cell-free culturefluids were prepared by removing the cells from the growth medium bycentrifugation at 15,000 rpm for 5 min in a microcentrifuge. The clearedculture fluids were passed through 0.2 μm HT Tuffryn filters (Gelman)and stored at −20° C. Cell-free culture fluids containing V. harveyiAutoinducer-2 were prepared from V. harveyi strain BB152 (Autoinducer1⁻, Autoinducer 2⁺). V. harveyi BB120 (Autoinducer 1⁺, Autoinducer 2⁺)was used to prepare culture fluids containing Autoinducer-1. In bothcases, the V. harveyi strains were grown overnight at 30° C. withaeration in AB (Autoinducer Bioassay) (Bassler et al., 1993, supra)medium. Cell-free culture fluids from V. harveyi were prepared from theovernight culture exactly as described above for E. coli and S.typhimurium.

Assay for Production of Signaling Molecules. Cell-free culture fluidsfrom E. coli, S. typhimurium and V. harveyi strains were tested for thepresence of signaling substances that could induce luminescence in theV. harveyi reporter strain BB170 or BB886. In the assays, 10 μl ofcell-free culture fluids from E. coli AB1157, E. coli DH5α, and S.typhimurium LT2 strains grown and harvested as described above wereadded to 96-well microtiter dishes. The V. harveyi reporter strain BB170or BB886 was grown for 16 h at 30° C. with aeration in AB medium,diluted 1:5000 into fresh AB medium, and 90 μl of the diluted cells wereadded to the wells containing the E. coli and S. typhimurium cell-freeculture fluids. Positive control wells contained 10 μl of cell-freeculture fluid from strain V. harveyi BB152 (Autoinducer-1⁻,Autoinducer-2⁺) or V. harveyi BB120 (Autoinducer-1⁺, Autoinducer-2⁺).Negative control wells contained 10 μl of sterile growth medium. Themicrotiter dishes were shaken in a rotary shaker at 175 rpm at 30° C.Every hour, light production was measured using a Wallac Model 1450Microbeta Plus liquid scintillation counter in the chemiluminescencemode. The V. harveyi cell density was measured by diluting the samealiquots of cells used for measuring luminescence, spreading thedilutions onto solid LM medium (Bassler et al., 1993, supra, incubatingthe plates overnight at 30° C., and counting the resulting colonies thefollowing day.

Preparation of E. coli and S. typhimurium Viable and UV-killed Cells forthe Activity Assay. E. coli AB1157, E. coli DH5α and S. typhimurium LT2cultures were grown for 8 h in LB containing 0.5% glucose at 30° C. withaeration. The cultures were subjected to centrifugation for 5 min at15,000 rpm in a microcentrifuge and the growth medium was removed fromthe cell pellets by aspiration. The cell pellets were resuspended in ABmedium and washed by vigorous mixing. The cells were again subjected tocentrifugation for 5 min at 15,000 rpm. The AB wash medium was removedand discarded and the cells were resuspended in fresh AB medium. Eachcell suspension was diluted to give 1×10⁶ cells/10 μl, and multiple 10μl aliquots were added to wells of microtiter dishes. Half of the cellaliquots were treated with short wavelength ultraviolet light for 15 minat a distance of 10 cm. This treatment was sufficient to kill all of thecells as judged by plating and incubating the UV-treated cells, andensuring that no growth occurred by the next day. 90 μl of the dilutedV. harveyi reporter strain BB170 was next added to the wells containingeither the viable or dead E. coli and S. typhimurium cells, and theactivity assay was carried out exactly as described in the previoussection.

Analysis of Glucose in S. typhimurium LT2 Culture Fluids. Glucoseconcentrations were determined in cell-free culture fluids prepared fromS. typhimurium using a Trinder assay (Diagnostic Chemicals Ltd.)according to the recommendations of the manufacturer, except that theglucose standards were prepared in LB medium. The assay was sensitive toless than 0.002% glucose. No interfering substances were present in LBmedium or spent LB culture fluids.

Bacterial Strains, Media and Recombinant DNA Techniques. V. harveyiBB120 is the wild type strain (Bassler et al., 1997, supra). S.typhimurium strain LT2 was obtained from Dr. K. Hughes (University ofWashington), S. typhimurium 14028 is ATCC strain 14028 Organism:Salmonella choleraesuis. E. coli O157:H7 is a clinical isolate suppliedby Dr. Paddy Gibb (University of Calgary). Luria broth (LB) contained 10g Bacto Tryptone (Difco), 5 g Yeast Extract (Difco) and 10 g NaCl perliter. The recipe for Autoinducer Bioassay (AB) medium has been reportedpreviously (Greenberg, E. P., Hastings, J. W., and Ulitzur, S. (1979)Arch. Microbiol. 120, 87-91). Where specified, glucose was added from asterile 20% stock to a final concentration of 0.5%. Antibiotics wereused at the following concentrations (mg/L): Ampicillin (Amp) 100,Chloramphenicol (Cm) 10, Gentamycin (Gn) 100, Kanamycin (Kn) 100, andTetracycline (Tet) 10. DNA isolation, restriction analysis andtransformation of E. coli was performed as described by Sambrook et at.Probes for Southern Blot analysis were labeled using the Multiprime DNAlabeling system of Amersham. Sequencing was carried out using an AppliedBiosystems sequencing apparatus. The V. harveyi BB120 genomic librarywas constructed in the cosmid pLAFR2 as described (Bassler et al., 1993,supra). The method for Tn5 mutagenesis of cloned V. harveyi genes, andthe allelic replacement technique for inserting Tn5 mutated genes intothe V. harveyi chromosome have been reported (Bassler et al., 1993,supra).

Bioluminescence Assay. The AI-2 bioassay using the V. harveyi reporterstrain BB170 (Sensor 1⁻, Sensor 2⁺) has been discussed in the previousexamples. Cell-free culture fluids from V. harveyi, E. coli, or S.typhimurium strains to be tested for AI-2 activity were prepared asdescribed above, and assayed at 10% (v/v). AI-2 activity is reported asthe fold-induction of the reporter strain over background, or as thepercent of the activity obtained from V. harveyi BB120 (wild type)cell-free culture fluid.

Mutagenesis and Analysis of the AI-2 Production Gene in S. typhimuriumLT2. MudJ insertion mutants of S. typhimurium LT2 were generated using aphage P22 delivery system as described (Maloy, S. R., Stewart, V. J.,and Taylor, R. K. (1996) Genetic analysis of pathogenic bacteria: alaboratory manual. Cold Spring Harbor Laboratory Press, Cold SpringHarbor, N.Y.). Following growth to mid-exponential phase in LBcontaining 0.5% glucose, the S. typhimurium insertion mutants weretested for AI-2 production using the V. harveyi BB170 bioassay. The siteof the MudJ insertion that inactivated the AI-2 production function inS. typhimurium was identified by PCR amplification and sequencing of thechromosomal DNA at the insertion junction. A two-step amplificationprocedure was used (Caetano-Annoles, G. (1993) Meth. Appl. 3, 85-92). Inthe first PCR reaction, the arbitrary primer5′-GGCCACGCGTCGACTAGTACNNNNNNNNNNACGCCC-3′, and the MudJ specific primer5′-GCACTACAGGCTTGCAAGCCC-3′ were used. Next, 1 μl of this PCR reactionwas used as the template in a second PCR amplification employing asecond arbitrary primer (5′-GGCCACGCGTCGACTAGTCA-3′) and another MudJspecific primer (5′-TCTAATCCCATCAGATCCCG-3′). The PCR product from thesecond reaction was purified and sequenced.

Cloning and Sequencing of the E. coli MG1655, E. coli O157:H7, and E.coli DH5α AI-2 Production Genes. The DNA sequence obtained from the S.typhimurium LT2 MudJ screen was used to search the E. coli MG1655 genomesequence to identify the corresponding E. coli region (Blattner et al.,Science 277, 1453-1462, 1997). The gene identified from the sequencingproject had the designation ygaG. Primers that flanked the ygaG gene andincorporated restriction sites were designed and used to amplify the E.coli MG1655, E. coli O157:H7 and E. coli DH5α ygaG genes. The primersused are: 5′-GTGAAGCTTGTTTACTGACTAGATC-3′ and5′-GTGTCTAGAAAAACACGCCTGACAG-3′. The PCR products were purified,digested, and cloned into pUC19. In each case, the PCR products fromthree independent reactions were cloned and sequenced.

The present invention is not limited to the embodiments described andexemplified above, but is capable of variation and modification withinthe scope of the appended claims.

27 1 519 DNA Vibrio harveyi 1 atgcctttat tagacagctt taccgtagaccacacgcgta tgaatgcacc agcggttcgt 60 gtggctaaaa cgatgcaaac tccaaaaggagacaccatca cggtattcga cctacgtttc 120 actgctccaa acaaagacat cctttctgagaaaggaattc atacattaga gcatttgtac 180 gcaggcttta tgcgtaatca cctaaatggtgatagcgttg agatcattga tatctcacca 240 atggggtgcc gtactggttt ctacatgagcttgattggta cgccttcaga gcagcaagtg 300 gctgacgctt ggattgccgc gatggaagacgtactaaaag tagaaaacca aaacaagatc 360 cctgagttga acgaatacca atgtggtacagcagcgatgc actctctgga tgaagcgaag 420 caaatcgcga agaacattct agaagtgggtgtggcggtga ataagaatga tgaattggca 480 ctgccagagt caatgctgag agagctacgcatcgactaa 519 2 516 DNA Escherichia coli 2 atgccgttgt tagatagcttcacagtcgat catacccgga tggaagcgcc tgcagttcgg 60 gtggcgaaaa caatgaacaccccgcatggc gacgcaatca ccgtgttcga tctgcgcttc 120 tgcgtgccga acaaagaagtgatgccagaa agagggatcc ataccctgga gcacctgttt 180 gctggtttta tgcgtaaccatcttaacggt aatggtgtag agattatcga tatctcgcca 240 atgggctgcc gcaccggtttttatatgagt ctgattggta cgccagatga gcagcgtgtt 300 gctgatgcct ggaaagcggcaatggaagac gtgctgaaag tgcaggatca gaatcagatc 360 ccggaactga acgtctaccagtgtggcact taccagatgc actcgttgca ggaagcgcag 420 gatattgcgc gtagcattctggaacgtgac gtacgcatca acagcaacga agaactggca 480 ctgccgaaag agaagttgcaggaactgcac atctag 516 3 110 DNA Salmonella typhimurium misc_feature(1)...(110) sequence from MudJ 3 gatgtgctga aagtgcagga tcaaaaccagatcccggagc tgaacgttta ccagtgcggt 60 acgtatcaga tgcactcgct cagtgaagcgcaggacattg cccgtcatat 110 4 492 DNA Salmonella typhimurium 4 aattcggatcataccggatg caagcgccgg cggtccgggt tgcaaaaacg atgaacaccc 60 cgcatggcgacgcaatcacg tgtttgatct gcgtttttgc attccgaaca aagaagtgat 120 gccggaaaaagggattcata cgcttgagca tctgtttgct ggctttatgc gcgaccacct 180 caacggtaacggcgttgaga ttatcgatat ctcgccgatg ggctgccgca ccggctttta 240 catgagcctgattggcacgc cggacgagca gcgtgttgcc gacgcctgga aagcggcgat 300 ggcggatgtgctgaaagtgc aggatcaaaa ccagatcccg gagctgaacg tttaccagtg 360 cggtacgtatcagatgcact cgctcagtga agcgcaggac attgcccgtc atattctgga 420 gcgtgatgtgcgcgtgaaca gcaataaaga gctggcgctg ccgaaagaaa aactgcagga 480 actgatattt ag492 5 504 DNA Haemophilus influenzae 5 atgccattac ttgatagttt taaagtggatcacacaaaaa tgaacgcacc tgcagtacgc 60 attgcaaaaa cgatgctcac gccaaaaggcgataatatta ctgtttttga tttacgtttt 120 tgtattccaa acaaagaaat tctttccccaaaaggcattc atacacttga acatttattt 180 gctggattta tgcgcgatca tttaaatggcgatagcatag aaattattga tatttctccg 240 atgggatgtc gcacgggatt ttatatgtctttgattggca caccaaatga acagaaagtg 300 tctgaggctt ggttagcttc aatgcaagatgttttaggtg tacaagatca agcttctatt 360 cctgaattaa atatctatca atgcggaagctatacggaac attccttaga agatgcacac 420 gaaattgcca aaaatgttat cgcacgcggtataggtgtaa ataaaaatga agatttgtca 480 ctcgataatt ccttattaaa atag 504 6468 DNA Helicobacter pylori 6 atgaaaacac caaaaatgaa tgtagagagttttaatttgg atcacaccaa agtcaaagcc 60 ccttatgtgc gtgtcgctga tcgcaaaaagggcgttaatg gggatttgat tgtcaaatac 120 gatgtgcgct tcaagcagcc caaccaagatcacatggaca tgcctagcct acattcttta 180 gagcatttag tcgctgaaat tatccgcaaccatgccagtt atgtcgtgga ttggtcgcct 240 atgggttgcc aaacgggatt ttatctcacagtgttaaacc atgacaatta cacagagatt 300 ttagaggttt tagaaaagac catgcaagatgtgttaaagg ctacagaagt gcctgccagc 360 aatgaaaagc aatgcggttg ggcggctaaccacactttag agggtgctaa ggatttagcg 420 cgcgcttttt tagacaaacg cgctgagtggtctgaagtgg gggtttga 468 7 482 DNA Bacillus subtilis 7 atgccttcagtagaaagttt tgagcttgat cataatgcgg ttgttgctcc atatgtaaga 60 cattgcggcgtgcataaagt gggaacagac ggcgttgtaa ataaatttga cattcgtttt 120 tgccagccaaataaacaggc gatgaagcct gacaccattc acacactcga gcatttgctc 180 gcgtttacgattcgttctca cgctgagaaa tacgatcatt ttgatatcat tgatatttct 240 ccaatgggctgccagacagg ctattatcta gttgtgagcg gagagccgac atcagcggaa 300 atcgttgatctgcttgaaga cacaatgaag gaagcggtag agattacaga aatacctgct 360 gcgaatgaaaagcagtgcgg ccaagcgaag cttcatgatc tggaaggcgc taaacgttta 420 atgcgtttctggctttcaca ggataaagaa gaattgctaa aagtatttgg ctaaaataga 480 aa 482 8 537DNA Borrelia burdorferi 8 atgaatttga atgggaaaaa ttagattttg taaaaaaaatacaaacagcg ctaaaaaaat 60 gaaaaaaata acaagcttta caatagatca tacaaaactcaaccctggca tatatgtctc 120 aagaaaagat acctttgaaa atgtaatatt tactacaatagacattagaa tcaaagctcc 180 caacatcgaa ccaataattg aaaacgcagc aatacatacaatagagcaca taggagctac 240 tttacttaga aataatgaag tttggaccga aaaaatagtatattttggcc ctatgggatg 300 cagaactggt ttttacttaa taatttttgg agactatgaaagtaaagatc ttgttgactt 360 agtctcatgg cttttttccg aaatcgtaaa tttttcagaacctatcccag gcgcaagtga 420 taaggaatgc ggaaattaca aagaacataa ccttgatatggctaaatatg aatcttctaa 480 atacttacaa atattaaaca atattaaaga agaaaatttaaaatatcctt agctcat 537 9 519 DNA Vibrio cholerae 9 atgccattat tagacagttttaccgtcgat catactcgta tgaatgcacc ggcggtgcgt 60 gttgccaaaa ccatgcaaaccccaaaaggg gatacgatta ccgtatttga tttgcgtttt 120 actatgccaa acaaagatatcttgtctgag cgcggtatcc atactctaga gcatctctac 180 gcgggcttta tgcgcaatcaccttaacggc agccaagtgg agatcatcga tatttcacca 240 atgggttgcc gtacaggtttctacatgagc ttgattggtg cgccgacaga acagcaagtg 300 gcacaagcat ggctagccgcaatgcaagat gtgttgaaag ttgaaagcca agagcaaatt 360 cctgagctga atgagtaccagtgcggcact gcggcgatgc actcgctcga agaagccaaa 420 gcgattgcga aaaacgtgattgcggcaggc atctcggtta accgtaacga tgagttggcg 480 ctgcccgaat ctatgctcaatgagctgaag gttcactaa 519 10 172 PRT Vibrio harveyi 10 Met Pro Leu LeuAsp Ser Phe Thr Val Asp His Thr Arg Met Asn Ala 1 5 10 15 Pro Ala ValArg Val Ala Lys Thr Met Gln Thr Pro Lys Gly Asp Thr 20 25 30 Ile Thr ValPhe Asp Leu Arg Phe Thr Ala Pro Asn Lys Asp Ile Leu 35 40 45 Ser Glu LysGly Ile His Thr Leu Glu His Leu Tyr Ala Gly Phe Met 50 55 60 Arg Asn HisLeu Asn Gly Asp Ser Val Glu Ile Ile Asp Ile Ser Pro 65 70 75 80 Met GlyCys Arg Thr Gly Phe Tyr Met Ser Leu Ile Gly Thr Pro Ser 85 90 95 Glu GlnGln Val Ala Asp Ala Trp Ile Ala Ala Met Glu Asp Val Leu 100 105 110 LysVal Glu Asn Gln Asn Lys Ile Pro Glu Leu Asn Glu Tyr Gln Cys 115 120 125Gly Thr Ala Ala Met His Ser Leu Asp Glu Ala Lys Gln Ile Ala Lys 130 135140 Asn Ile Leu Glu Val Gly Val Ala Val Asn Lys Asn Asp Glu Leu Ala 145150 155 160 Leu Pro Glu Ser Met Leu Arg Glu Leu Arg Ile Asp 165 170 11171 PRT Escherichia coli 11 Met Pro Leu Leu Asp Ser Phe Thr Val Asp HisThr Arg Met Glu Ala 1 5 10 15 Pro Ala Val Arg Val Ala Lys Thr Met AsnThr Pro His Gly Asp Ala 20 25 30 Ile Thr Val Phe Asp Leu Arg Phe Cys ValPro Asn Lys Glu Val Met 35 40 45 Pro Glu Arg Gly Ile His Thr Leu Glu HisLeu Phe Ala Gly Phe Met 50 55 60 Arg Asn His Leu Asn Gly Asn Gly Val GluIle Ile Asp Ile Ser Pro 65 70 75 80 Met Gly Cys Arg Thr Gly Phe Tyr MetSer Leu Ile Gly Thr Pro Asp 85 90 95 Glu Gln Arg Val Ala Asp Ala Trp LysAla Ala Met Glu Asp Val Leu 100 105 110 Lys Val Gln Asp Gln Asn Gln IlePro Glu Leu Asn Val Tyr Gln Cys 115 120 125 Gly Thr Tyr Gln Met His SerLeu Gln Glu Ala Gln Asp Ile Ala Arg 130 135 140 Ser Ile Leu Glu Arg AspVal Arg Ile Asn Ser Asn Glu Glu Leu Ala 145 150 155 160 Leu Pro Lys GluLys Leu Gln Glu Leu His Ile 165 170 12 164 PRT Salmonella typhimurium 12Asn Ser Asp His Thr Arg Met Gln Ala Pro Ala Val Arg Val Ala Lys 1 5 1015 Thr Met Asn Thr Pro His Gly Asp Ala Ile Thr Val Phe Asp Leu Arg 20 2530 Phe Cys Ile Pro Asn Lys Glu Val Met Pro Glu Lys Gly Ile His Thr 35 4045 Leu Glu His Leu Phe Ala Gly Phe Met Arg Asp His Leu Asn Gly Asn 50 5560 Gly Val Glu Ile Ile Asp Ile Ser Pro Met Gly Cys Arg Thr Gly Phe 65 7075 80 Tyr Met Ser Leu Ile Gly Thr Pro Asp Glu Gln Arg Val Ala Asp Ala 8590 95 Trp Lys Ala Ala Met Ala Asp Val Leu Lys Val Gln Asp Gln Asn Gln100 105 110 Ile Pro Glu Leu Asn Val Tyr Gln Cys Gly Thr Tyr Gln Met HisSer 115 120 125 Leu Ser Glu Ala Gln Asp Ile Ala Arg His Ile Leu Glu ArgAsp Val 130 135 140 Arg Val Asn Ser Asn Lys Glu Leu Ala Leu Pro Lys GluLys Leu Gln 145 150 155 160 Glu Thr Asp Ile 13 167 PRT Haemophilusinfluenzae 13 Met Pro Leu Leu Asp Ser Phe Lys Val Asp His Thr Lys MetAsn Ala 1 5 10 15 Pro Ala Val Arg Ile Ala Lys Thr Met Leu Thr Pro LysGly Asp Asn 20 25 30 Ile Thr Val Phe Asp Leu Arg Phe Cys Ile Pro Asn LysGlu Ile Leu 35 40 45 Ser Pro Lys Gly Ile His Thr Leu Glu His Leu Phe AlaGly Phe Met 50 55 60 Arg Asp His Leu Asn Gly Asp Ser Ile Glu Ile Ile AspIle Ser Pro 65 70 75 80 Met Gly Cys Arg Thr Gly Phe Tyr Met Ser Leu IleGly Thr Pro Asn 85 90 95 Glu Gln Lys Val Ser Glu Ala Trp Leu Ala Ser MetGln Asp Val Leu 100 105 110 Gly Val Gln Asp Gln Ala Ser Ile Pro Glu LeuAsn Ile Tyr Gln Cys 115 120 125 Gly Ser Tyr Thr Glu His Ser Leu Glu AspAla His Glu Ile Ala Lys 130 135 140 Asn Val Ile Ala Arg Gly Ile Gly ValAsn Lys Asn Glu Asp Leu Ser 145 150 155 160 Leu Asp Asn Ser Leu Leu Lys165 14 155 PRT Helicobacter pylori 14 Met Lys Thr Pro Lys Met Asn ValGlu Ser Phe Asn Leu Asp His Thr 1 5 10 15 Lys Val Lys Ala Pro Tyr ValArg Val Ala Asp Arg Lys Lys Gly Val 20 25 30 Asn Gly Asp Leu Ile Val LysTyr Asp Val Arg Phe Lys Gln Pro Asn 35 40 45 Gln Asp His Met Asp Met ProSer Leu His Ser Leu Glu His Leu Val 50 55 60 Ala Glu Ile Ile Arg Asn HisAla Ser Tyr Val Val Asp Trp Ser Pro 65 70 75 80 Met Gly Cys Gln Thr GlyPhe Tyr Leu Thr Val Leu Asn His Asp Asn 85 90 95 Tyr Thr Glu Ile Leu GluVal Leu Glu Lys Thr Met Gln Asp Val Leu 100 105 110 Lys Ala Thr Glu ValPro Ala Ser Asn Glu Lys Gln Cys Gly Trp Ala 115 120 125 Ala Asn His ThrLeu Glu Gly Ala Lys Asp Leu Ala Arg Ala Phe Leu 130 135 140 Asp Lys ArgAla Glu Trp Ser Glu Val Gly Val 145 150 155 15 157 PRT Bacillus subtilis15 Met Pro Ser Val Glu Ser Phe Glu Leu Asp His Asn Ala Val Val Ala 1 510 15 Pro Tyr Val Arg His Cys Gly Val His Lys Val Gly Thr Asp Gly Val 2025 30 Val Asn Lys Phe Asp Ile Arg Phe Cys Gln Pro Asn Lys Gln Ala Met 3540 45 Lys Pro Asp Thr Ile His Thr Leu Glu His Leu Leu Ala Phe Thr Ile 5055 60 Arg Ser His Ala Glu Lys Tyr Asp His Phe Asp Ile Ile Asp Ile Ser 6570 75 80 Pro Met Gly Cys Gln Thr Gly Tyr Tyr Leu Val Val Ser Gly Glu Pro85 90 95 Thr Ser Ala Glu Ile Val Asp Leu Leu Glu Asp Thr Met Lys Glu Ala100 105 110 Val Glu Ile Thr Glu Ile Pro Ala Ala Asn Glu Lys Gln Cys GlyGln 115 120 125 Ala Lys Leu His Asp Leu Glu Gly Ala Lys Arg Leu Met ArgPhe Trp 130 135 140 Leu Ser Gln Asp Lys Glu Glu Leu Leu Lys Val Phe Gly145 150 155 16 173 PRT Borrelia burgdorferi 16 Met Gly Lys Ile Arg PheCys Lys Lys Asn Thr Asn Ser Ala Lys Lys 1 5 10 15 Met Lys Lys Ile ThrSer Phe Thr Ile Asp His Thr Lys Leu Asn Pro 20 25 30 Gly Ile Tyr Val SerArg Lys Asp Thr Phe Glu Asn Val Ile Phe Thr 35 40 45 Thr Ile Asp Ile ArgIle Lys Ala Pro Asn Ile Glu Pro Ile Ile Glu 50 55 60 Asn Ala Ala Ile HisThr Ile Glu His Ile Gly Ala Thr Leu Leu Arg 65 70 75 80 Asn Asn Glu ValTrp Thr Glu Lys Ile Val Tyr Phe Gly Pro Met Gly 85 90 95 Cys Arg Thr GlyPhe Tyr Leu Ile Ile Phe Gly Asp Tyr Glu Ser Lys 100 105 110 Asp Leu ValAsp Leu Val Ser Trp Leu Phe Ser Glu Ile Val Asn Phe 115 120 125 Ser GluPro Ile Pro Gly Ala Ser Asp Lys Glu Cys Gly Asn Tyr Lys 130 135 140 GluHis Asn Leu Asp Met Ala Lys Tyr Glu Ser Ser Lys Tyr Leu Gln 145 150 155160 Ile Leu Asn Asn Ile Lys Glu Glu Asn Leu Lys Tyr Pro 165 170 17 172PRT Vibrio cholerae 17 Met Pro Leu Leu Asp Ser Phe Thr Val Asp His ThrArg Met Asn Ala 1 5 10 15 Pro Ala Val Arg Val Ala Lys Thr Met Gln ThrPro Lys Gly Asp Thr 20 25 30 Ile Thr Val Phe Asp Leu Arg Phe Thr Met ProAsn Lys Asp Ile Leu 35 40 45 Ser Glu Arg Gly Ile His Thr Leu Glu His LeuTyr Ala Gly Phe Met 50 55 60 Arg Asn His Leu Asn Gly Ser Gln Val Glu IleIle Asp Ile Ser Pro 65 70 75 80 Met Gly Cys Arg Thr Gly Phe Tyr Met SerLeu Ile Gly Ala Pro Thr 85 90 95 Glu Gln Gln Val Ala Gln Ala Trp Leu AlaAla Met Gln Asp Val Leu 100 105 110 Lys Val Glu Ser Gln Glu Gln Ile ProGlu Leu Asn Glu Tyr Gln Cys 115 120 125 Gly Thr Ala Ala Met His Ser LeuGlu Glu Ala Lys Ala Ile Ala Lys 130 135 140 Asn Val Ile Ala Ala Gly IleSer Val Asn Arg Asn Asp Glu Leu Ala 145 150 155 160 Leu Pro Glu Ser MetLeu Asn Glu Leu Lys Val His 165 170 18 32 DNA Artificial Sequenceoligonucleotide primer for fts Q1P promoter 18 cggagatctg cgctttcaatggataaacta cg 32 19 30 DNA Artificial Sequence oligonucleotide primerfor fts Q2P promoter 19 cgcggatcct cttcttcgct gtttcgcgtg 30 20 36 DNAArtificial Sequence oligonucleotide primer 20 ggccacgcgt cgactagtacnnnnnnnnnn acgccc 36 21 21 DNA Artificial Sequence MudJ specificoligonucleotide primer 21 gcactacagg cttgcaagcc c 21 22 20 DNAArtificial Sequence arbitrary oligonucleotide primer 22 ggccacgcgtcgactagtca 20 23 20 DNA Artificial Sequence MudJ specificoligonucleotide primer 23 tctaatccca tcagatcccg 20 24 25 DNA ArtificialSequence oligonucleotide primer 24 gtgaagcttg tttactgact agatc 25 25 25DNA Artificial Sequence oligonucleotide primer 25 gtgtctagaa aaacacgcctgacag 25 26 171 PRT Escherichia coli 26 Met Pro Leu Leu Asp Ser Phe ThrVal Asp His Thr Arg Met Glu Ala 1 5 10 15 Pro Ala Val Arg Val Ala LysThr Met Asn Thr Pro His Gly Asp Ala 20 25 30 Ile Thr Val Phe Asp Leu ArgPhe Cys Val Pro Asn Lys Glu Val Met 35 40 45 Pro Glu Arg Gly Ile His ThrLeu Glu His Leu Phe Ala Gly Phe Met 50 55 60 Arg Asn His Leu Asn Gly AsnGly Val Glu Ile Ile Asp Ile Ser Pro 65 70 75 80 Met Gly Cys Arg Thr GlyPhe Tyr Met Ser Leu Ile Gly Thr Pro Asp 85 90 95 Glu Gln Arg Val Ala AspAla Trp Lys Ala Ala Met Glu Asp Val Leu 100 105 110 Lys Val Gln Asp GlnAsn Gln Ile Pro Glu Leu Asn Val Tyr Gln Cys 115 120 125 Gly Thr Tyr GlnMet His Ser Leu Gln Glu Ala Gln Asp Ile Ala Arg 130 135 140 Ser Ile LeuGlu Arg Asp Val Arg Ile Asn Ser Asn Glu Glu Leu Ala 145 150 155 160 LeuPro Lys Glu Lys Leu Gln Glu Leu His Ile 165 170 27 111 PRT Escherichiacoli 27 Met Pro Leu Leu Asp Ser Phe Thr Val Asp His Thr Arg Met Glu Ala1 5 10 15 Pro Ala Val Arg Val Ala Lys Thr Met Asn Thr Pro His Gly AspAla 20 25 30 Ile Thr Val Phe Asp Leu Arg Phe Cys Val Pro Asn Lys Glu ValMet 35 40 45 Pro Glu Arg Gly Ile His Thr Leu Glu His Leu Phe Ala Gly PheMet 50 55 60 Arg Asn His Leu Asn Gly Asn Gly Val Glu Ile Ile Asp Ile SerPro 65 70 75 80 Met Gly Cys Arg Thr Gly Phe Tyr Met Ser Leu Leu Val ArgGln Met 85 90 95 Ser Ser Val Leu Leu Met Pro Gly Lys Arg Gln Trp Lys ThrCys 100 105 110

What is claimed is:
 1. A method for regulating the activity of anautoinducer-2 receptor comprising contacting an autoinducer-2 receptorwith an AI-2 agonist or antagonist compound.
 2. The method of claim 1,wherein the compound has the structure:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond; or

wherein C² is additionally bonded to at least one substituent selectedfrom hydrogen, hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅ alkanoyl, C₂₋₅alkanoyloxy, heteroaryl, or forms a double bond with an oxygen atom orC³; wherein C³ is additionally bonded to at least one substituentselected from hydrogen, hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅alkanoyl, C₂₋₅ alkanoyloxy, or forms a double bond with an oxygen atomor C²; wherein C⁴ is additionally bonded to at least one substituentselected from hydrogen, C₁₋₅ alkyl, C₂₋₅ alkanoyl, C₂₋₅ alkanoyloxy, orforms a double bond with an oxygen atom or C⁵; and wherein C⁵ isadditionally bonded to at least one substituent selected from hydrogen,C₁₋₅ alkyl, C₂₋₅ alkanoyl, C₂₋₅ alkanoyloxy, or forms a double bond withan oxygen atom or C⁴, wherein at least one of C², C³, C⁴ or C⁵ is bondedto a substituent selected from hydroxyl, C₁₋₅ alkyl, C₂₋₅ alkenyl, C₂₋₅alkanoyl, and heteroaryl, and wherein at most one carbon-carbondouble-bond is present in the ring; or

wherein R is a C₁₋₅ alkoxyl group.
 3. The method of claim 1 wherein theautoinducer-2 receptor is selected from the group consisting of LuxP andLuxQ.
 4. The method of claim 3 wherein the autoinducer-2 receptor isLuxP.
 5. The method of claim 3 wherein the autoinducer-2 receptor isLuxQ.
 6. The method of claim 1, wherein the AI-2 receptor is found on abacterial cell.
 7. The method of claim 6, wherein the bacterial cell isfound in a warm blooded host.
 8. The method of claim 7, wherein theactivity regulated is bacterial cell growth.
 9. The method of claim 8,wherein the compound is of the formula:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 10. The method of claim 9, wherein the compound is of theformula:


11. The method of claim 8, wherein the bacterial cell is selected fromthe group consisting of Vibrio harveyi, Vibrio cholerae, Vibrioparahaemolyticus, Vibrio alginolyticus, Pseudomonas phosphoreum,Yersinia enterocolitica, Escherichia coli, Salmonella typhimurium,Haemophilus influenzae, Helicobacter pylori, Bacillus subtilis, Borreliaburgfdorferi, Neisseria meningitidis, Neisseria gonorrhoeae, Yersiniapestis, Campylobacter jejuni, Deinococcus radiodurans, Mycobacteriumtuberculosis, Enterococcus faecalis, Streptococcus pneumoniae,Streptococcus pyogenes and Staphylococcus aureus.
 12. The method ofclaim 6, wherein the activity is bacterial virulence.
 13. The method ofclaim 12, wherein the compound is of the formula:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 14. The method of claim 13, wherein the compound is of theformula:


15. The method of claim 13, wherein the bacterial cell is chosen fromthe group consisting of Vibrio harveyi, Vibrio cholerae, Vibrioparahaemolyticus, Vibrio alginolyticus, Pseudomonas phosphoreum,Yersinia enterocolitica, Escherichia coli, Salmonella typhimurium,Haemophilus influenzae, Helicobacter pylori, Bacillus subtilis, Borreliaburgfdorferi, Neisseria meningitidis, Neisseria gonorrhoeae, Yersiniapestis, Campylobacter jejuni, Deinococcus radiodurans, Mycobacteriumtuberculosis, Enterococcus faecalis, Streptococcus pneumoniae,Streptococcus pyogenes and Staphylococcus aureus.
 16. The method ofclaim 6, wherein the activity is siderophore expression.
 17. The methodof claim 16, wherein the activity is the inhibition of siderophoreexpression.
 18. The method of claim 16, wherein the compound is of theformula:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 19. The method of claim 16, wherein the bacterial cell ischosen from the group consisting of Vibrio harveyi, Vibrio cholerae,Vibrio parahaemolyticus, Vibrio alginolyticus, Pseudomonas phosphoreum,Yersinia enterocolitica, Escherichia coli, Salmonella typhimurium,Haemophilus influenzae, Helicobacter pylori, Bacillus subtilis, Borreliaburgfdorferi, Neisseria meningitidis, Neisseria gonorrhoeae, Yersiniapestis, Campylobacter jejuni, Deinococcus radiodurans, Mycobacteriumtuberculosis, Enterococcus faecalis, Streptococcus pneumoniae,Streptococcus pyogenes and Staphylococcus aureus.
 20. The method ofclaim 6, wherein the activity regulated is exopolysaccharide productionin bacterial cells.
 21. The method of claim 20, wherein theexopolysaccharide production is rugose polysaccharide production. 22.The method of claim 20, wherein the compound is of the formula:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 23. The method of claim 6, wherein the activity regulatedis bacterial colony morphology.
 24. The method of claim 23, wherein theactivity regulated is smooth colony morphology formation.
 25. The methodof claim 24, wherein the bacterial cell is a pathogenic bacterial cell.26. The method of claim 23, wherein the compound is of the structure:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen; R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 27. The method of claim 6, wherein the activity regulatedis biofilm formation.
 28. The method of claim 27, wherein the compoundis of the formula:

wherein X is oxygen, sulfur or nitrogen; R_(1a) is hydrogen, hydroxy,alkyl, acyl, amido, hydroxyl, amino, thio, or aryl; R_(1b) is hydrogen,hydroxy, alkyl, acyl, amido, hydroxyl, amino, mercapto, thio, or aryl,or R_(1a) and R_(1b) can together form a double bond; R₂ is hydrogen,alkyl, or halogen, R₃ is hydrogen, alkyl, acyl, amido, hydroxyl, amino,thio, or aryl; R₄ is hydrogen, if X is nitrogen, or is absent if X isoxygen or sulfur; and wherein C₄ and C₅ can be further joined by adouble bond.
 29. The method of claim 28, wherein the compound is of theformula: